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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415978Generated: October 30, 2026

Boron tribromide → 1-Cyclohexyl-3-(2,6-dichloro-4-hydroxy-benzyl)-pyrrolidin-2-one

https://huagongshe.com/reaction/415978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Cyclohexyl-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-oneHCID 59299414—
SolventDichloromethaneHCID 6344—
Product1-Cyclohexyl-3-(2,6-dichloro-4-hydroxy-benzyl)-pyrrolidin-2-oneHCID 5929942212.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 1-cyclohexyl-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one (86 g, 241.4 mmol) in 1300 mL dichloromethane then cool to 0° C. under nitrogen. Slowly add BBr3 (120.9 g, 482.75 mmol) to the stirring cold solution keeping the internal temperature below 3.5° C. Stir the solution cold for ˜2 hours, then pour into 4 L of saturated sodium bicarbonate and stir rapidly for ˜20 minutes. Filter and wash the solid with water, then air dry on the funnel. Separate the organic portion of the filtrate and wash with water then brine. Dry over sodium sulfate, filter and concentrate under vacuum. Suspend the resultant tan solid in dichloromethane, filter, wash the solid with dichloromethane and dry to yield 10.5 g of off-white solid. Combine all solids and dry over night in a vacuum oven at 45° C. to yield 78.6 g (95%) of a light-tan solid: MS: (m/z) 342 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088776B2
Source datasetuspto-grants-2012_01
ORD IDord-8b5f8e9b51b247e6ad09f09cf313cd18
Source noteuspto-grants-2012_01