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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917333Generated: November 1, 2026

Benzyl Alcohol → HCID 12151386, compound

https://huagongshe.com/reaction/917333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12151385HCID 12151385—
SolventDimethylformamideHCID 6228—
ProductHCID 12151386HCID 1215138676.5%

Reaction Steps

Into 3 ml of N,N-dimethylformamide were dissolved 416 mg of 5-chloro-3-(4-chlorobenzylthio)-1,2,4-thiadiazole and 162 mg of benzyl alcohol, 48 mg of sodium hydride (60% in oil) was added thereto under ice-cooling, and the reaction mixture was stirred for 15 minutes under ice-cooling and for 1 hour at room temperature. The reaction mixture was added to saturated sodium chloride aqueous solution, and extracted with t-butyl methyl ether. The organic layer was concentrated, and the residue obtained was subjected to silica gel column chromatography to give 400 mg of 5-benzyloxy-3-(4-chlorobenzyl)thio-1,2,4-thiadiazole (hereinafter, referred to as the present compound (32)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273879B2
Source datasetuspto-grants-2007_09
ORD IDord-b31dbf901ecc4e3fa3b9e1ee47378e14
Source noteuspto-grants-2007_09