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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411264Generated: October 30, 2026

Boron tribromide → HCID 90449646, compound

https://huagongshe.com/reaction/1411264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 90449880HCID 90449880—
SolventDichloromethaneHCID 6344—
ProductHCID 90449646HCID 9044964691%

Reaction Conditions

Temperature-20 °C

Reaction Steps

1-(1′-Acetyl-5-methoxyspiro[indoline-3,3′-pyrrolidin]-1-yl)-2,2,2-trifluoroethanone (2.74 g, 8.00 mmol) was dissolved in methylene chloride (50 mL). Thereafter, 1 M boron tribromide (40 mL, 40.0 mmol) was added to the above obtained solution at −78° C., and the thus obtained mixture was then stirred at −20° C. for 3 hours. Thereafter, the reaction solution was poured into ice water, and was then extracted with chloroform. The organic layer was washed with water and brine, and was then dried over anhydrous sodium sulfate, followed by concentration in vacuo. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=20:1) to obtain 1-(1′-acetyl-5-hydroxyspiro[indoline-3,3′-pyrrolidin]-1-yl)-2,2,2-trifluoroethanone (2.39 g, 91%) in the form of a dark brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-262beddee4ac4c0f8ded3adb2f660e13
Source noteuspto-grants-2014_12