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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261273Generated: November 2, 2026

Bromotrichloromethane → HCID 67234103, compound

https://huagongshe.com/reaction/2261273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrichloromethaneHCID 6383—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 43405688HCID 43405688—
SolventDichloromethaneHCID 6344—
ProductHCID 67234103HCID 67234103—

Reaction Conditions

Temperature-78 °C

Reaction Steps

DAST (diethylaminosulfur trifluoride) was added to a cold (−78° C.) solution of 3-hydroxy-2-[2-(4-methoxy-phenyl)-acetylamino]-propanoic acid methyl ester (400 mg, 1.5 mmol) in dichloromethane (8 mL). After stirring for 1 h at −78° C., CCl3Br (149 μL, 1.5 mmol) and DBU (226 μL, 1.5 mmol) were added and the reaction was allowed to warm to 25° C. and stirred at this temperature for 12 h. The reaction was poured into saturated aqueous NaHCO3 and the biphasic mixture was extracted with DCM. The combined organic extracts were dried with MgSO4 and purified by column chromatography (hexanes:ethyl acetate from 25 to 100%). 2-(4-Methoxy-benzyl)-oxazole-4-carboxylic acid methyl ester was isolated as a white solid (80 mg, 21%). ESI-MS m/z calc. 247.5, found 248.2 (M+1)+. Retention time of 2.64 minutes. 1H NMR (400 MHz, CDCl3) δ 3.80 (s, 3H), 3.92 (s, 3H), 4.12 (s, 2H), 6.87 (d, J=8.0 Hz, 2H), 7.24 (d, J=8.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846951B2
Source datasetuspto-grants-2010_12
ORD IDord-b845fa69d0d742a791edaff00e44da53
Source noteuspto-grants-2010_12