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

1,2-Dichloroethane → 1,3,3-Trimethyl-2-oxabicyclo(2.2.2)octan-6-one

HRID 426576
노트
인쇄 미리보기

반응식

HRID 426576 반응식
[CH3:1][C:2]1[CH2:7][CH2:6][C@H:5]([C:8]([OH:11])([CH3:10])[CH3:9])[CH2:4][CH:3]=1.ClC1C=CC=C(C(OO)=[O:20])C=1.C(Cl)CCl.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>C(Cl)Cl>[CH3:1][C:2]12[CH2:7][CH2:6][CH:5]([CH2:4][C:3]1=[O:20])[C:8]([CH3:10])([CH3:9])[O:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 111,2-DichloroethaneHCID 70297m-Chloroperbenzoic acidHCID 443162(L)-alpha-terpineolHCID 178418287HCID 178418287, 화합물

생성물 1

HCID 1122031,3,3-Trimethyl-2-oxabicyclo(2.2.2)octan-6-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 3.08 g. (0.02 mole) α-terpineol and 4.45 g. (0.022 mole) of 85 percent m-chloroperbenzoic acid in 70 ml. of ethylene dichloride is refluxed under nitrogen for 20 hours, then cooled to room temperature and washed with aqueous sodium bisulfite and sodium bicarbonate solutions. The solvent is removed in vacuo and the resulting oil is treated in situ with 2.94 g. (0.0136 mole) pyridinium chlorochromate. The resulting mixture is stirred under nitrogen in 35 ml. of methylene chloride at ambient temperatures for 2.5 hours. After addition of 200 ml. diethyl ether, the mixture is filtered through celite and the solvent evaporated to give, on steam distillation, 1,3,3-trimethyl-2-oxabicyclo [2,2,2]octan-6-one; m.p. 50° to 52° C.

후처리

  1. additionA mixture of 3.08 g
  2. washwashed with aqueous sodium bisulfite and sodium bicarbonate solutions
  3. customThe solvent is removed in vacuo
  4. additionthe resulting oil is treated in situ with 2.94 g
  5. additionAfter addition of 200 ml
  6. filtrationdiethyl ether, the mixture is filtered through celite
  7. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-f5359b997e454ac181e33e29059008cf
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04170599

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트