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Ethyl Bromide → 1H-Imidazole, 2-(2-benofuranyl)-1-ethyl-, monohydrochloride

HRID 1707663
Notes
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Reaction equation

HRID 1707663 reaction equation
[ClH:1].[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH:4]=[C:3]1[C:11]1[NH:12][CH:13]=[CH:14][N:15]=1.[CH2:16](Br)[CH3:17]>>[ClH:1].[CH2:16]([N:15]1[CH:14]=[CH:13][N:12]=[C:11]1[C:3]1[O:2][C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH:4]=1)[CH3:17]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6332Ethyl BromideHCID 30735951H-Imidazole, 2-(2-benzofuranyl)-, monohydrochloride

Product 1

HCID 30736031H-Imidazole, 2-(2-benofuranyl)-1-ethyl-, monohydrochloride

Procedure

This was prepared from 2-(benzofuran-2-yl)imidazole hydrochloride and ethyl bromide according to the procedure of example 2; m.p.=183°-185° C.

Sources & evidence

ORD record
ord-0305071cb6ac4b57848bfaa1279d0a87
Source dataset
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05354769

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes