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Benzyl Alcohol → Benzyl 6-hydroxyhexanoate

HRID 486168
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인쇄 미리보기

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HRID 486168 반응식
[C:1]1(=[O:8])[O:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:9]([OH:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[OH:8][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]([O:16][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 244Benzyl AlcoholHCID 10401epsilon-CAPROLACTONEHCID 521998p-Toluenesulfonic acid monohydrate

생성물 1

HCID 15224618Benzyl 6-hydroxyhexanoate

반응 조건

온도
100 °C

실험 절차

A mixture of ε-caprolactone (a) (40 g), benzyl alcohol and p-toluenesulfonic acid monohydrate (0.7 g) was stirred at 100° C. for 16 hours. The reaction mixture was treated in the conventional manner and was distilled under reduced pressure (1 mmHg, 140°-154° C.) to give the title compound (b).

후처리

  1. additionThe reaction mixture was treated in the conventional manner
  2. distillationwas distilled under reduced pressure (1 mmHg, 140°-154° C.)

출처 및 근거

ORD 기록
ord-8701ea7f45784dd9bbd5c83a8eb7bd79
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05290811

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