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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227900Generated: October 30, 2026

Benzaldehyde → HCID 11731822, compound

https://huagongshe.com/reaction/2227900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11808112HCID 11808112—
SolventDichloromethaneHCID 6344—
ProductHCID 11731822HCID 11731822—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under argon atmosphere, in 3 ml of methylene chloride was dissolved 141 mg (0.5 mmol) of 3-diphenylmethyl-5-methoxy-2(3H)oxazolone, and after cooling the solution to −78° C., 53.1 mg (0.5 mmol) of benzaldehyde and 0.05 ml (0.05 mmol) of a methylene chloride solution containing 1.0 M-trimethylsilyl triflate were added to the solution and the mixture was reacted under stirring for one hour. After the temperature of the mixture was raised up to 0° C., 15 ml of a saturated aqueous sodium hydrogen carbonate solution was added to the resulting reaction mixture and the mixture was extracted with 20 ml of methylene chloride. The organic layer was washed with 15 ml of a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 184 mg (0.476 mmol) of 3-diphenylmethyl-4-methoxycarbonyl-5-phenyl-2-oxzolidinone as white crystal. (Yield based on 3-diphenylmethyl-5-methoxy-2(3H)oxazolone: 95%.) According to HPLC analysis, a formation ratio of cis/trans-isomers of the formed product was 5/95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414160B1
Source datasetuspto-grants-2002_07
ORD IDord-ce3e7e053f2f4bb3b69a65d30f4b276b
Source noteuspto-grants-2002_07