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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905098Generated: November 1, 2026

Triethylamine → HCID 56634706, compound

https://huagongshe.com/reaction/1905098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant4-Acetoxy-2-azetidinoneHCID 119981—
ReactantHCID 56611923HCID 56611923—
SolventDichloromethaneHCID 6344—
ProductHCID 56634706HCID 5663470630%

Reaction Steps

1.8 ml (13.0 mmol - 2.6 equivalents) of triethylamine and then 2.3 ml (12.0 mmol - 2.4 equivalents) of trimethylsilyl trifluoromethanesulphonate were added to a solution, which had been cooled to 0° C., of 646 mg (5.0 mmol) of 4-acetoxy-2-azetidinone and 1.42 g (6.5 mmol) of tert.-butyl 4-chloro-2-diazo-3-oxobutanoate in 45 ml of anhydrous dichloromethane. The cooling bath was removed and the mixture was stirred at room temperature for 5 h, then 0.3 ml (1.5 mmol - 0.3 equivalent) of trimethylsilyl trifluoromethanesulphonate was added and the mixture was stirred at room temperature for 1 h. To work up, it was poured into a mixture of cold saturated NaHCO3 solution and ethyl acetate, extraction with ethyl acetate was carried out, and the organic extracts were washed with saturated NaCl solution and dried over MgSO4. After evaporation of the solvent in vacuo and chromatography on 40 g of silica gel (toluene:ethyl acetate 1:1), 426 mg (30%) of the title compound were obtained as a mixture of diastereomers (10:1), Rf: 0.35 (toluene:ethyl acetate 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841042
Source datasetuspto-grants-1989_06
ORD IDord-129091a8d0d741d6a344fc0c321ee91b
Source noteuspto-grants-1989_06