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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → 2H-Indeno[2,1-d]oxazol-2-one, 3,3a,4,8b-tetrahydro-, cis-

HRID 965226
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HRID 965226 반응식
Cl[C@@H:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][C@H:3]1[NH:11][C:12]([O:14]C(C)(C)C)=[O:13].C(OCC)C>C(Cl)(Cl)Cl>[O:13]1[C@H:2]2[C:10]3[C:5]([CH2:4][C@H:3]2[NH:11][C:12]1=[O:14])=[CH:6][CH:7]=[CH:8][CH:9]=3
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참가 물질

4

반응물 2

HCID 3283Diethyl EtherHCID 18661305(+/-)trans-1-Chloro-2-tert-butoxycarbonylaminoindane

생성물 1

HCID 867528562H-Indeno[2,1-d]oxazol-2-one, 3,3a,4,8b-tetrahydro-, cis-수율 92.6%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of (±) trans-1-chloro-2-tert-butoxycarbonylaminoindane (10.0 g, 0.037 mol) in chloroform (200 ml) was heated under reflux in an argon atmosphere for 23 h. The mixture was concentrated in vacuo to give a brown solid. Trituration with diethyl ether afforded the title compound as a beige solid (6.0 g, 92%) m.p. 205°-206° C. which was used without further purification.

후처리

  1. temperatureunder reflux in an argon atmosphere for 23 h
  2. concentrationThe mixture was concentrated in vacuo
  3. customto give a brown solid

출처 및 근거

ORD 기록
ord-5b8611b88a6e4c3d9cd3615833de6fae
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773463

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