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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758821Generated: October 27, 2026

1,4-Dioxane → (2R,3S,5R,6R) 2-Carbamoyloxymethyl-2-methyl-6-(2-phenoxyacetamido)penam-3-carboxylic Acid p-Nitrobenzyl Ester

https://huagongshe.com/reaction/1758821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantTrichloroacetyl isocyanateHCID 76400—
Reactant(1S,3S,5R,6R) 2,2-dimethyl-6-phenoxyacetamidopenam-3-carboxylic acid-1-oxide p-nitrobenzyl esterHCID 11145535—
Product(2R,3S,5R,6R) 2-Carbamoyloxymethyl-2-methyl-6-(2-phenoxyacetamido)penam-3-carboxylic Acid p-Nitrobenzyl EsterHCID 12817536—

Reaction Steps

A solution of (1S,3S,5R,6R) 2,2-dimethyl-6-phenoxyacetamidopenam-3-carboxylic acid-1-oxide p-nitrobenzyl ester (7.52 g, 15.0 mmol) and trichloroacetyl isocyanate (5.0 ml, 7.9 g, 42 mmol) in dioxane (75 ml) was refluxed under nitrogen for 3.5 hours and concentrated in vacuo. The concentrate was stirred with methanol (100 ml) and the solution was decanted from a black tar with methanol rinses (2×10 ml). The solution was diluted with water (5 ml), adjusted to pH 7.4 with 5% sodium bicarbonate, and held at pH 7.4-7.5 with 3% H2SO4 for 2.5 hours. The mixture was distributed between methylene chloride (100 ml) and water (50 ml). The organic phase was washed with water (50 ml), combined with a CH2Cl2 back extract (50 ml), dried (4A molecular sieve), polish filtered with CH2Cl2 washes (2×20 ml), and concentrated in vacuo to a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374982
Source datasetuspto-grants-1983_02
ORD IDord-60650632b7d84d1b8df59e9e8bb35370
Source noteuspto-grants-1983_02