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Phenolphthalein → Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester

HRID 392537
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HRID 392537 반응식
[OH-].[Na+].[Br-].[C:4]([CH2:9][P+:10]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([O:6][CH2:7][CH3:8])=[O:5].C1C=CC2C(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)OC(=O)C=2C=1>O.C(Cl)(Cl)Cl>[C:4]([CH:9]=[P:10]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)([O:6][CH2:7][CH3:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 4764PhenolphthaleinHCID 14798Sodium HydroxideHCID 73731(Ethoxycarbonylmethyl)triphenylphosphonium bromide

생성물 1

HCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester수율 90%

시약·촉매·용매 2

HCID 962Water용매HCID 6212
Chloroform
용매
2회

실험 절차

Ethyl bromoacetate (14.4 g, 0.094 mol) was added dropwise over 30 min to a stirred solution of 26.2 g (0.1 mol) of triphenylphosphine in 120 ml of benzene maintained at 35 38° C. After stirring for additional 12 h at room temperature the precipitate was filtered and washed twice with hexane to give 34.7 g (86%) of (carboethoxymethyl)-triphenylphosphonium bromide, m.p. 159 160° C. 115 ml of 10% aqueous sodium hydroxide was added dropwise with cooling at 5° C. to a stirred suspension of 118.4 g (0.276 mol) of the bromide in 500 ml of water and 200 ml of chloroform containing a small amount of phenolphthalein. Stirring was continued over 30 min period without external cooling followed by adding 500 ml of chloroform to give clear layers. The aqueous layer was extracted three times with 100 ml of chloroform and the combined chloroform fractions were dried over sodium sulfate and concentrated in vacuo. Crystallization of the residue from 180 ml of 1:1 mixture of benzene and hexane gave 86.1 g (90%) of pure (carboethoxymethylene)triphenylphosphorane, m.p. 119 120° C.

후처리

  1. custom159 160° C
  2. temperaturewithout external cooling
  3. customto give clear layers
  4. extractionThe aqueous layer was extracted three times with 100 ml of chloroform
  5. dry with materialthe combined chloroform fractions were dried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customCrystallization of the residue
  8. additionfrom 180 ml of 1:1 mixture of benzene and hexane

출처 및 근거

ORD 기록
ord-ea9e83d94eec41a1841c7e1d06fc3989
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06800772B2

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