Allyl Alcohol → HCID 21558585, compound

HRID 1578725Notes

Reaction equation

HRID 1578725 reaction equation
Cl[C:2]1[C:10]2[NH:9][C:8]([CH:11]([F:13])[F:12])=[N:7][C:6]=2[C:5]([N+:14]([O-:16])=[O:15])=[CH:4][C:3]=1[C:17]#[N:18].[Na].[CH2:20]([OH:23])[CH:21]=[CH2:22]>>[CH2:20]([O:23][C:2]1[C:10]2[NH:9][C:8]([CH:11]([F:13])[F:12])=[N:7][C:6]=2[C:5]([N+:14]([O-:16])=[O:15])=[CH:4][C:3]=1[C:17]#[N:18])[CH:21]=[CH2:22]

Participants

4

Reactant 3

HCID 7858Allyl AlcoholHCID 5360545SodiumHCID 135783928HCID 135783928, compound

Product 1

HCID 21558585HCID 21558585, compound

Procedure

4-Chloro-7-nitro-5-cyano-2-difluoromethylbenzimidazole is reacted with the sodium salt of allyl alcohol to obtain 4-allyloxy-7-nitro-5-cyano-2-difluoromethylbenzimidazole, m.w., 294.2.

Sources & evidence

ORD record
ord-6e055e5e8c74485ab37fa3f3f5e5a889
Source dataset
uspto-grants-1976_02
Patent number
US03939166

Reaction notes

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