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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584233Generated: October 30, 2026

Carbon tetrabromide → HCID 54394904, compound

https://huagongshe.com/reaction/584233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
Reactant1,1-Dimethylethyl (3S)-3-formyl-4-morpholinecarboxylateHCID 44182322—
SolventDichloromethaneHCID 6344—
ProductHCID 54394904HCID 54394904—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphenylphosphine (7.31 g) was added to a solution of carbon tetrabromide (4.62 g) in dichloromethane (15 ml) at 0° C. and the mixture was stirred at 0° C. for 15 minutes. A solution of (3S)-4-tert-butoxycarbonyl-3-formylmorpholine (1.5 g) in dichloromethane (15 ml) was added dropwise to the solution over 10 minutes at 0° C. and stirred for 3 hours, and the mixture was added saturated sodium hydrogen carbonate solution. The organic layer was separated and the aqueous layer was extracted with ethyl acetate three times. The combined organic layer was washed with brine, dried over magnesium sulfate, and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of ethyl acetate and n-hexane (4:6) to give (3R)-4-tert-butoxycarbonyl-3-(2,2-dibromoethenyl)morpholine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-a34b36a575984e14b7139396428f6dc5
Source noteuspto-grants-2005_08