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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isobutyric Acid → Ethyl 5,9-dimethyl-3,4,8-decatrienoate

HRID 1284164
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HRID 1284164 반응식
[C:1]([O-:7])([O-])([O:3][CH2:4][CH3:5])[CH3:2].[CH3:8][C:9]([CH3:18])=[CH:10][CH2:11][CH2:12][C:13](O)([C:15]#[CH:16])[CH3:14].C(O)(=O)C(C)C>>[CH3:14][C:13]([CH2:12][CH2:11][CH:10]=[C:9]([CH3:18])[CH3:8])=[C:15]=[CH:16][CH2:2][C:1]([O:3][CH2:4][CH3:5])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6590Isobutyric AcidHCID 62842DehydrolinaloolHCID 86598186Ethyl ortho-acetate

생성물 1

HCID 21515741Ethyl 5,9-dimethyl-3,4,8-decatrienoate수율 96%

실험 절차

A mixture of 65.6 g of ethyl ortho-acetate, 30.4 g of dehydrolinalool and 1.5 g of isobutyric acid was reacted at 130° to 140°C. for 8 hours. Distillation was conducted after the reaction in the same manner as in the preceeding Examples, and a fraction boiling at 92 to 94°C. under 0.5 mm Hg was collected. Ethyl 5,9-dimethyl-3,4,8-decatrienoate was obtained in a yield of 96%.

후처리

  1. customwas reacted at 130° to 140°C. for 8 hours
  2. distillationDistillation
  3. customafter the reaction in the same manner as in the preceeding Examples
  4. customa fraction boiling at 92 to 94°C. under 0.5 mm Hg was collected

출처 및 근거

ORD 기록
ord-c7c8fa9fee444d038d342260fae3be70
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03978100

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