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Benzyl Alcohol → 2-(Benzyloxy)propanoic acid

HRID 65191
노트
인쇄 미리보기

반응식

HRID 65191 반응식
CCOCC.[Na].Cl[CH:8]([CH3:12])[C:9]([OH:11])=[O:10].[CH2:13]([OH:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH2:13]([O:20][CH:8]([CH3:12])[C:9]([OH:11])=[O:10])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 244Benzyl Alcohol2회HCID 3283Diethyl EtherHCID 117342-Chloropropionic acidHCID 5360545Sodium2회

생성물 1

HCID 2459872-(Benzyloxy)propanoic acid

반응 조건

온도
150 °C

실험 절차

An alternate method for the preparation of ether compounds corresponding to Formula I (R=alkyl, phenylalkyl) follows. Sodium metal (about 12 g) was added cautiously to a stirred cold (ice bath) portion (250 mL) of benzyl alcohol. After most of the sodium metal had dissolved, the reaction was heated to 150° C. 2-Chloropropionic acid (27.2 g, 0.25 mole) was added dropwise in 35 mL of benzyl alcohol and the resulting mixture heated on additional 3 hours. Concentration in vacuo gave crude 2-benzyloxypropionic acid which was used without further purification.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturethe resulting mixture heated on additional 3 hours
  2. concentrationConcentration in vacuo

출처 및 근거

ORD 기록
ord-fe9164041aa440dc9fdedea83fb7fb30
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04613600

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