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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604625Generated: October 25, 2026

Carbon tetrabromide → 2-(Bromomethyl)-3-chloro-1-benzothiophene

https://huagongshe.com/reaction/604625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(3-Chloro-1-benzothien-2-yl)methanolHCID 821965—
SolventDichloromethaneHCID 6344—
Product2-(Bromomethyl)-3-chloro-1-benzothiopheneHCID 816708—

Reaction Steps

A solution of triphenylphosphine (1.74 g, 6.62 mmol) in dry CH2Cl2 (6 mL) was added dropwise to a stirred solution of carbon tetrabromide (2.20 g, 6.62 mmol) and (3-chloro-1-benzothien-2-yl)methanol (0.94 g, 4.73 mmol) in dry CH2Cl2 (35 mL) at 0° C. under N2. The reaction was allowed to warm to room temperature and was stirred for 4 h then concentrated in vacuo to give the crude product. This was purified by flash chromatography (Si, 40×160 nm, 0-25% EtOAc in hexanes gradient) to afford 2-(bromomethyl)-3-chloro-1-benzothiophene. Rf=0.93 (20% EtOAc/hexanes). 1H NMR (600 MHz, CDCl3): δ 7.81 (dd, J=1.3, 7-1 Hz, 1H); 7.78 (dd, J=1.2, 7.2 Hz, 1H); 7.47-7.41 (m, 2H); 4.81 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-b34e4a9d8d7b4538832fea2ce15af53d
Source noteuspto-grants-2011_03