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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422269Generated: October 25, 2026

Triphenylphosphine → 4-(Bromomethyl)-2-phenylthiazole

https://huagongshe.com/reaction/422269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant4-(Hydroxymethyl)-2-phenyl-1,3-thiazoleHCID 2776473—
SolventDichloromethaneHCID 6344—
Product4-(Bromomethyl)-2-phenylthiazoleHCID 6659849293.8%

Reaction Conditions

Temperature-6 °C

Reaction Steps

Bromine (177 mg, 1.1 mmol) was added directly into a solution of triphenylphosphine (288 mg, 1.1 mmol) in DCM (2 mL) to give a kind of white precipitate. The temperature was cooled to −6° C. A solution of commercially available (2-phenylthiazol-4-yl)methanol (200 mg, 1.04 mmol) in DCM (1 mL) was added dropwise. The resulting mixture was maintained at −6° C. for 15 min and then warmed to room temperature for 1 h. A white precipitate was formed. The solution was filtered and the white precipitate was washed with DCM. The white precipitate was collected and dissolved in NaHCO3 0.5M After 30 min of stirring, the aqueous layer was extracted with DCM and the organic phase was washed with water, dried over MgSO4, filtered and evaporated to afford 248 mg of 4-(bromomethyl)-2-phenylthiazole (Yield: 71%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-0a799c9dc1084987af96466ffa2117f7
Source noteuspto-grants-2012_01