CAS: 1700-37-4; 3-Benzyloxybenzaldehyde

相似化合物

1700-30-7 69026-14-8 61147-43-1

上下游产品

CAS号100-39-0 溴化苄 | CAS号100-83-4 间羟基苯甲醛 | CAS号100-44-7 氯化苄 | CAS号591-31-1 3-甲氧基苯甲醛 | CAS号1700-30-7 3-苄氧基苯甲醇 | CAS号22272-48-6 3-苯甲基酚 | CAS号100-51-6 苯甲醇 | CAS号93033-58-0 3-(BENZYLOXY)BE... | CAS号19438-10-9 间羟基苯甲酸甲酯 | CAS号79678-37-8 3-(苄氧基)苯甲酸甲酯 | CAS号104566-43-0 3-苄氧基苄胺 | CAS号588-05-6 3-(2-氨基乙基)苯酚 | CAS号3769-41-3 3-苄氧基苯酚 | CAS号51061-22-4 3-苯氧基苯乙胺 | CAS号57668-34-5 3-[3-(Benzyloxy... | CAS号30798-64-2 1,2,3,4-四氢异喹啉-7-醇 | CAS号37951-47-6 3′-苄氧基丙苯酮 | CAS号501-24-6 3-十五烷基苯酚 | CAS号91523-50-1 6-羟基-1,2,3,4-四氢... | CAS号188576-49-0 叔丁基 7-羟基-3,4-二氢...

N-[(3-Phenylmethoxyphenyl)Methylideneamino]Aniline置于水,Phosphorus Pentoxide体系中,化学反应 0.01H,以72%的收率获得3-苄氧基苯甲醛
参考文献:Banerjee,Krishna; Mitra,Alok Kumar,Journal Of The Indian Chemical Society,2003,Vol. 80,# 3,P. 184-186
标题:Banerjee,Krishna; Mitra,Alok Kumar,Journal Of The Indian Chemical Society,2003,Vol. 80,# 3,P. 184-186

专利信息

专利号:US-5861532-A
优先权日:1997-03-04
标 题:Solid-phase synthesis of N-alkyl amides
发明人：BROWN EDWARD G; NUSS JOHN M
权利人:CHIRON CORP
摘要:Methods for solid phase synthesis of N-alkyl amides comprise reductive amination of carbonyl compounds using a reducing agent and an amine-containing linker bound to a solid support. The methods afford high yields of linker-bound, monoalkylated amines, and subsequent coupling with acid derivatives provide derivatized N-substituted amides in excellent yields after cleavage from the solid-phase. Compositions useful in solid phase synthesis are also described.

专利号:US-9611206-B2
优先权日:2011-03-02
标题:Synthesis of intermediate for treprostinil production
发明人：SHARMA VIJAY
权利人:UNITED THERAPEUTICS CORP
摘要:The compound according to Formula I is an intermediate in the synthesis of prostacylin analogs. The present invention provides an efficient method for synthesizing a Formula I compound.

专利号:US-5175302-A
优先权日:1987-07-13
标 题 :Nucleophilic fluoroalkylation of aldehydes
发明人：STAHLY G PATRICK
权利人:ETHYL CORP
摘要:Aryl difluoromethyl sulfone adds to aldehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.

专利号:US-6482950-B1
优先权日:1991-05-06
标 题 :Squarylium compounds, and processes and intermediates for the synthesis of these compounds
发明人：GARCIA PAULINA P; LEE JOHN W; MARSHALL JOHN L; MCGOWAN DONALD A; PUTTICK ANTHONY J; SPENCER THOMAS K; STROUD STEPHEN G; TELFER STEPHEN J; ZURAW MICHAEL J
权利人:POLAROID CORP
摘要:Squarylium compounds of the formula: n wherein Q 1 and Q 2 are each independently a pyrylium, thiopyrylium, selenopyrylium, benzpyrylium, benzthiopyrylium or benzselenopyrylium nucleus, and R 1 and R 2 are each independently an aliphatic or cycloaliphatic group, can be prepared by reacting a squaric acid derivative of the formula: n with a compound of the formula Q 2 CH 2 R 2 in the presence of a base. The derivatives of Formula II may be prepared by condensing a 2,3,4,4-tetrahalocyclobut-2-en-1-one with a compound of the formula Q 1 CH 2 R 1 in the presence of a base to produce a compound of the formula: n wherein Q 1 and R 1 are as defined above, and X represents chlorine or bromine, and hydrolyzing the compound of Formula III. Alternatively, the derivatives of Formula II may be prepared by reacting a diester, monoacid chloride monoester or diacid chloride of squaric acid with a compound of the formula Q 1 CH 2 R 1 in the presence of a base, followed by hydrolysis of the resultant monoacid chloride or monoester derivative of the compound of Formula II to the parent compound.

专利号:US-4837327-A
优先权日:1987-07-13
标 题 :Process for nucleophilic fluoroalkylation of aldehydes
发明人：STAHLY G PATRICK
权利人:ETHYL CORP
摘要:Aryl difluoromethyl sulfone adds to alkehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.

专利号:US-4999429-A
优先权日:1989-01-09
标 题 :Process for the preparation of α,α,β-1-trifluoro-1-olefinic derivatives
发明人：STAHLY G PATRICK
权利人:ETHYL CORP
摘要:Aryl difluoromethyl sulfone adds to aldehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.