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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177259Generated: October 30, 2026

HCID 617437, compound → HCID 90418369, compound

https://huagongshe.com/reaction/2177259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 617437HCID 617437—
SolventChlorobenzeneHCID 7964—
ProductHCID 90418369HCID 90418369—

Reaction Conditions

Temperature50 °C

Reaction Steps

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 3-chloro-5-phenyl-1,2-thiazole-4-carboxylic acid (500 mg, 1.88 mmol, 1.00 equiv, 90%), chlorobenzene (2 mL), BH3 (3.1 mL, 3.00 equiv) at 0° C. The resulting solution was stirred for 12 h at 50° C. in an oil bath. The reaction was then quenched by the addition of 10 mL of sodium bicarbonate/H2O. The resulting solution was extracted with 3×10 mL of ethyl acetate and the organic layers combined. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:4). This resulted in 80 mg (18%) of (3-chloro-5-phenyl-1,2-thiazol-4-yl)methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-d270127c3a554186b9ffa26e82b57fef
Source noteuspto-grants-2015_06