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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850371Generated: October 30, 2026

Acetonitrile → 5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/1850371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantN-bromobutanimideHCID 67184—
Reactant2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuranHCID 11745437—
SolventWaterHCID 962—
Product5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuranHCID 6676092886%

Reaction Steps

N-bromosuccinimide (12.5 g, 70.0 mmol) was added to a solution of acetonitrile (165 mL) containing 2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran (11.1 g, 58.3 mmol) synthesized in Reference Example 3 under ice-cooling condition, and the mixture was warmed to room temperature. After stirring for 5 hours, water was added to the reaction solution. The generated precipitate was collected by filtration and washed with a mixture of acetonitrile/water (1/2). The solid was dried to give 13.5 g of the title compound (yield: 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957069B2
Source datasetuspto-grants-2015_02
ORD IDord-68e6d64275b441dc99a0b8d2cc5cc951
Source noteuspto-grants-2015_02