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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-isopropyl-2-trimethylsilyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide → 1-isopropyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide

HRID 2058900
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인쇄 미리보기

반응식

HRID 2058900 반응식
[CH:1]([P:4]1(=[O:17])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[CH2:6][N:5]1[Si](C)(C)C)([CH3:3])[CH3:2]>CO>[CH:1]([P:4]1(=[O:17])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[CH2:6][NH:5]1)([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 205484461-isopropyl-2-trimethylsilyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide

생성물 1

HCID 130375011-isopropyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The 1-isopropyl-2-trimethylsilyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide was added to 50 ml. of methanol and allowed to stand for 40 hours. The methanol was removed under vacuum and the resulting residue was slurried in ether to yield 1-isopropyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide as a white solid. A second crop was obtained to give a total yield of 2.35 g (20% yield) of 1-isopropyl-2,3-dihydro-1H-2,1-benzazaphosphole-1-oxide having a melting point of 149°-151° C. and the following analysis:

후처리

  1. customThe methanol was removed under vacuum

출처 및 근거

ORD 기록
ord-4ab7571b684a43d2864cbf25f6dd8b7f
출처 데이터셋
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04319913

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