Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649269Generated: October 31, 2026

Triethylamine → 2-Benzhydryloxycarbonyl-7-t-butoxycarbonylamino-3-(2-chlorovinyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-5-oxide

https://huagongshe.com/reaction/1649269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Benzhydryloxycarbonyl-7-t-butoxycarbonylamino-3-(2,2-dichloroethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-5-oxideHCID 13078707—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Benzhydryloxycarbonyl-7-t-butoxycarbonylamino-3-(2-chlorovinyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-5-oxideHCID 53780699100.2%

Reaction Steps

A solution of 2-benzhydryloxycarbonyl-7-t-butoxycarbonylamino-3-(2,2-dichloroethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-5-oxide (product 11f) (3.3 g) and triethylamine (0.88 cc) in dry tetrahydrofuran (50 cc) is stirred at 25° C. for 16 hours and the reaction mixture is then diluted with ethyl acetate (200 cc). The organic solution is washed with distilled water (5×60 cc), dried over sodium sulphate and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 35° C. This yields a product (11e) (3.1 g) in the form of a hard orange foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415562
Source datasetuspto-grants-1983_11
ORD IDord-d79d2e8b96624d8f8f0b690305e7f37f
Source noteuspto-grants-1983_11