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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537979Generated: October 27, 2026

Carbon tetrabromide → 5-(Bromomethyl)-6-iodoindane

https://huagongshe.com/reaction/537979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(6-iodo-2,3-dihydro-1H-inden-5-yl)methanolHCID 57576294—
SolventDichloromethaneHCID 6344—
Product5-(Bromomethyl)-6-iodoindaneHCID 57544355100.6%

Reaction Steps

To a solution of (6-iodo-2,3-dihydro-1H-inden-5-yl)methanol (36 mg, 0.131 mmol) and carbon tetrabromide (52 mg, 0.158 mmol) in dichloromethane (1 mL) at 0° C. under N2, was added triphenylphosphine (41 mg, 0.158 mmol). The resulting solution was allowed to warm to room temperature and was stirred for 4 h. Another portion of carbon tetrabromide (52 mg, 0.158 mmol) and triphenylphosphine (41 mg, 0.158 mmol) was added to the mixture at 0° C. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo. The residue was purified by flash chromatography (Si, 1% EtOAc in hexanes) to afford 5-(bromomethyl)-6-iodoindane (44.4 mg, 100%). 1H NMR (500 MHz, CDCl3) δ 7.72 (s, 1H), 7.36 (s, 1H), 4.62 (s, 2H), 2.89 (m, 4H), 2.11-2.07 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865707B2
Source datasetuspto-grants-2014_10
ORD IDord-86457f6cb62446a99e73e74ba87d1d9d
Source noteuspto-grants-2014_10