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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220304Generated: November 1, 2026

Diisobutylaluminumhydride → Benzo[b]thiophene, 7-fluoro-4-methoxy-

https://huagongshe.com/reaction/2220304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant7-fluoro-4-methoxy-1-benzothiophen-2(3H)-oneHCID 23568963—
SolventDichloromethaneHCID 6344—
ProductBenzo[b]thiophene, 7-fluoro-4-methoxy-HCID 2217114087.4%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of 7-fluoro-4-methoxy-1-benzothiophen-2(3H)-one (1.06, 5.4 mmol) in dichloromethane (10 mL) at 0° C. was added slowly a solution of diisobutylaluminium hydride in dichloromethane (1 M, 8.04 mL, 8.0 mmol). After 30 mins the reaction was quenched by careful addition of aqueous hydrochloric acid (6 N, 25 mL). The mixture was concentrated to remove the dichloromethane, the aqueous residue was then stirred at 35° C. for 2 h. The aqueous solution was extracted with diethyl ether (3×50 mL), washed with aqueous sodium hydroxide (2 N, 50 mL), brine (50 mL) then dried (MgSO4) and the solvent evaporated in vacuo to give the title compound (0.86 g, 87%) as a purple oil; δH 7.44-7.38 (1H, m, ArH), 7.36-7.24 (1H, m, ArH), 6.88-6.80 (1H, m, ArH), 6.57-6.49 (1H, m, ArH) and 3.82 (3H, s, OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417064B2
Source datasetuspto-grants-2008_08
ORD IDord-7bf3b3cd5781498a9af258dfc5d68e90
Source noteuspto-grants-2008_08