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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293110Generated: October 31, 2026

Ammonium Chloride → 2-(3-Chloro-propyl)-5-fluoro-3-methyl-benzo[b]thiophene

https://huagongshe.com/reaction/1293110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactant5-Fluoro-3-methyl-benzo[b]thiopheneHCID 596828—
ReactantButyllithiumHCID 178418339—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Chloro-propyl)-5-fluoro-3-methyl-benzo[b]thiopheneHCID 2298954537.1%

Reaction Conditions

Temperature-15 °C

Reaction Steps

n-BuLi in heptanes (1.5 ml, 2.4 mmol, 1.6M) was added drop wise to 5-fluoro-3-methyl-benzo[b]thiophene (332 mg, 2.0 mmol) in THF (5 ml) at −20° C. under argon. The reaction mixture was stirred at −15° C. for 30 min, then 1-chloro-3-iodopropane (322 μl, 3.0 mmol) and copper (1) iodide (38 mg, 0.2 mmol) were added. The reaction was stirred at −15° C. for 1 h, then NH4Cl (sat'd aq., 5 ml) was added. The product was extracted with diethyl ether (2×30 ml) and the organic layer was washed with brine (10 ml), dried (K2CO3), filtered and concentrated in vacuo. The product was purified by column chromatography (0–1% diethyl ether in heptanes) to give 2-(3-chloro-propyl)-5-fluoro-3-methyl-benzo[b]thiophene (180 mg, 37%). 1H NMR (CDCl3): δ 2.19 (tt, 2H), 2.22 (s, 3H), 2.94 (t, 2H), 3.57 (t, 2H), 7.04 (dt, 1H), 7.28 (dd, 1H), 7.66 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238713B2
Source datasetuspto-grants-2007_07
ORD IDord-09ee98683c5246b983551dd95d3c07a8
Source noteuspto-grants-2007_07