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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109772Generated: October 30, 2026

Carbon tetrabromide → 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromide

https://huagongshe.com/reaction/1109772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl alcoholHCID 53637583—
SolventTetrahydrofuranHCID 8028—
Product3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromideHCID 1901947171.9%

Reaction Steps

To a solution of 1.04 g of 3-(5-fluorobenzothiazol-2-ylmethoxy)benzyl alcohol (Preparation L) in 60 ml of dry tetrahydrofuran was added 2.38 g of carbontetrabromide and 1.89 g of triphenylphosphine and the reaction stirred under nitrogen at room temperature for 1.5 hours. The reaction mixture was filtered, treated with 100 ml of water and extracted with ethyl acetate. The extracts were washed with water and a brine solution and dried over sodium sulfate. The solvent was removed and the residual brown solid chromatographed on 200 g of silica gel using from 5-10% ethyl acetate--95-90% hexane (v:v). The fractions containing the product were combined and concentrated to give 910 mg of the titled product, m.p. 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322847
Source datasetuspto-grants-1994_06
ORD IDord-08744490abca494ba1deba0146110a81
Source noteuspto-grants-1994_06