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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040022Generated: October 25, 2026

Bromine → (5-Bromothiazol-2-yl)dicyclopropylmethanol

https://huagongshe.com/reaction/1040022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
ReactantDicyclopropyl(1,3-thiazol-2-yl)methanolHCID 49962381—
SolventAcetic AcidHCID 176—
Product(5-Bromothiazol-2-yl)dicyclopropylmethanolHCID 6742927357.1%

Reaction Steps

Bromine (0.271 mL, 5.26 mmol) was added dropwise to a stirred mixture of the product of Step 1 (411 mg, 2.10 mmol) and NaOAc (863 mg; 10.5 mmol) in acetic acid (9.17 mL) and the mixture was stirred at room temperature for 4 h. The reaction was quenched with brine and the aqueous layer was extracted with ethyl acetate (3×). The combined organics were washed with brine, dried (sodium sulfate), filtered, and concentrated. The residue was purified by chromatography on silica gel (0-100% ethyl acetate in hexanes) to give (5-bromo-1,3-thiazol-2-yl)(dicyclopropyl)methanol (329 mg, 1.20 mmol, 57% yield) as an off-white solid. MS APCI: [M-OH]+ m/z 255.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551984B2
Source datasetuspto-grants-2013_10
ORD IDord-fbcb113af19f4fcfb477c9f9934fa0fc
Source noteuspto-grants-2013_10