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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
Notes
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Reaction equation

HRID 2058900 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

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:

Workup

  1. customThe methanol was removed under vacuum

Sources & evidence

ORD record
ord-4ab7571b684a43d2864cbf25f6dd8b7f
Source dataset
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04319913

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes