Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723101Generated: November 1, 2026

Thionyl Chloride → HCID 178432159, compound

https://huagongshe.com/reaction/1723101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178432211HCID 178432211—
ProductHCID 178432159HCID 17843215986.8%

Reaction Steps

(b-1) A mixture of 13 parts of α-(3-fluorophenyl)-2-methyl-1H-benzimidazole-5-methanol monohydrochloride and 81 parts of thionyl chloride was stirred overnight at room temperature. The reaction mixture was concentrated to dry, yielding 12 parts (86.8%) of 5-[chloro(3-fluorophenyl)methyl]-2-methyl-1H-benzimidazole monohydrochloride as a residue (int. 45).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859684
Source datasetuspto-grants-1989_08
ORD IDord-fb8f6744abc14f34a0f833edd5b97cd8
Source noteuspto-grants-1989_08