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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965295Generated: November 1, 2026

Carbon tetrabromide → HCID 67357394, compound

https://huagongshe.com/reaction/1965295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 65426139HCID 65426139—
SolventDichloromethaneHCID 6344—
ProductHCID 67357394HCID 6735739497.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (7-fluorobenzofuran-2-yl)methanol (1.38 g, 8.31 mmol), tetrabromomethane (4.41 g, 13.3 mmol) and triphenylphosphine (2.61 g, 9.97 mmol) in dichloromethane (42 mL) was stirred at 0° C. for 2 h and concentrated in vacuo to dryness. The residue was purified by column chromatography (hexanes/ethyl acetate, 49/1) to afford 2-(bromomethyl)-7-fluorobenzofuran (1.85 g, 97%) as a colorless solid: 1H NMR (300 MHz, CDCl3) δ7.34-7.29 (m, 1H), 7.20-7.12 (m, 1H), 7.10-7.02 (m, 1H), 6.82-6.77 (m, 1H), 4.60 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-197139ad014147dca959f6bdfb9859d0
Source noteuspto-grants-2013_04