Trityl chloride → N-Triphenylmethyl-5-benzyl-tetrazole

Reaction equation

[CH2:1]([C:8]1[NH:12][N:11]=[N:10][N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:13]1([C:19](Cl)([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[C:13]1([C:19]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:12]2[C:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[N:9][N:10]=[N:11]2)[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Participants

Reactant 2

HCID 6456Trityl chloride

HCID 178420213HCID 178420213, compound

Product 1

HCID 22407523N-Triphenylmethyl-5-benzyl-tetrazole

Procedure

Prepared from 5-benzyl-1H-tetrazole and triphenylmethyl-chloride.

Sources & evidence

ORD record: ord-5b436bc6e8ad4cc1813694c6453c2149
Source dataset: uspto-grants-1996_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05519138

Reaction notes

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