홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

3a,4,5,7a-Tetrahydro-2-benzofuran-1,3-dione → 3-Cyclohexene-1,2-dicarboxylic acid

HRID 1577041
노트
인쇄 미리보기

반응식

HRID 1577041 반응식
[CH2:1]=[CH:2][CH:3]=[CH:4][CH2:5][CH2:6][CH:7]([OH:9])[CH3:8].[C:10]1(=[O:20])[O:15][C:13](=[O:14])[CH:12]2[CH2:16][CH2:17][CH:18]=[CH:19][CH:11]12>C([O-])(=O)C.[Zn+2].C([O-])(=O)C.C1(C)C(C)=CC=CC=1>[CH2:1]=[CH:2][CH:3]=[CH:4][CH2:5][CH2:6][CH:7]([OH:9])[CH3:8].[C:10]([OH:15])(=[O:20])[CH:11]1[CH:19]=[CH:18][CH2:17][CH2:16][CH:12]1[C:13]([OH:9])=[O:14]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 127266013a,4,5,7a-Tetrahydro-2-benzofuran-1,3-dioneHCID 572477947-Octadienol

생성물 2

HCID 127266073-Cyclohexene-1,2-dicarboxylic acidHCID 572477947-Octadienol

시약·촉매·용매 2

HCID 11192Zinc Acetate촉매2회HCID 7237O-Xylene용매

실험 절차

In a 1 liter glass autoclave equipped with a thermometer, a condenser, a nitrogen gas inlet and a stirrer, 378 g. (3.0 mole) of 2, 7 - octadienol - 1, 152 g. (1.0 mole) of tetrahydrophthalic anhydride, 100 ml. of xylene and 0.5g. of zinc acetate 2 - hydrate were charged. In accordance with the process of Reference Example 1, 388 g of the di-(2, 7 - octadienol - 1) ester of tetrahydrophthalic acid was obtained as the product.

출처 및 근거

ORD 기록
ord-53e235e243144e55bbdb0b8b0b7d28ac
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03983289

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트