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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592834Generated: October 30, 2026

Carbon tetrabromide → HCID 58610157, compound

https://huagongshe.com/reaction/1592834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 58610153HCID 58610153—
ReactantHCID 58610189HCID 58610189—
SolventDichloromethaneHCID 6344—
ProductHCID 58610157HCID 5861015734%
ProductHCID 58610179HCID 58610179—

Reaction Steps

A solution of carbon tetrabromide (3.3 g, 9.96 mmol) in dichloromethane (4 ml) was added dropwise over 5 min to a stirred solution of (R)-[3-fluorophenyl][(2R)-4-benzylmorpholin-2-yl]methanol and (S)-[3-fluorophenyl][(2S)-4-benzylmorpholin-2-yl]methanol (2.0 g, 6.64 mmol) and triphenylphosphine (2.61 g, 9.96 mmol) in dichloromethane (40 ml) at room temperature under nitrogen. After 30 min, the reaction solution was washed with saturated aqueous sodium bicarbonate (50 ml). The dichloromethane layer was dried, filtered and evaporated to a red liquid (8.5 g). Trituration with diethyl ether (40 ml) crystallised triphenylphoshine oxide that was then removed by filtration. The filtrate was evaporated to a yellow oil and was purified by chromatography on silica eluting with ethyl acetate:hexane 20:80 to give a colourless oil of (2R)-2-[(S)-bromo(3-fluorophenyl)methyl]-4-benzylmorpholine and (2S)-2-[(R)-bromo(3-fluorophenyl)methyl]-4-benzylmorpholine (0.811 g, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294623B2
Source datasetuspto-grants-2007_11
ORD IDord-b9ac7801d3e64fa282406bed553f8429
Source noteuspto-grants-2007_11