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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439265Generated: October 30, 2026

3-(Trimethylsilyl)oxazolidin-2-one → 7-Aminodeacetoxycephalosporanic acid

https://huagongshe.com/reaction/1439265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trimethylsilyl)oxazolidin-2-oneHCID 123514—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with N,N-diethylethanamine (1:1)HCID 161127—
ReactantThioureaHCID 2723790—
Reactant4-Methylbenzene-1-sulfonic acid--N,N-dimethylaniline (1/1)HCID 71353520—
Product7-Aminodeacetoxycephalosporanic acidHCID 33498347.7%

Reaction Steps

To the above solution, there were added 0.28 mole of 3-trimethylsilyl-2-oxazolidinone (TMSO, 38.2 ml) and 0.02 mole of triethylamine p-toluenesulphonate (8.468 g). After stirring for 15 minutes, the mixture was heated under reflux for 120 minutes. Thereafter 0.1 mole of dimethylaniline p-toluene sulphonate (29.3 g) and 0.12 mole of thiourea (9.13 g) were added and heating was maintained for a further 60 minutes. Thereafter the mixture was concentrated at reduced pressure and water (100 ml) was added to the residue. The pH was adjusted to 8.5 in the presence of methylene chloride, the phenyl-pseudothio-hydantoin was filtered out and the water phase was decanted off. After further adjustment To pH 4.2, the mixture was filtered again to give 7-ADCA (14.9 g) with 70% yield. Identified by its IR spectrum, m.p. 232- 42 (d) and [α] D2 = 105.0° (C = 1%, 0.5 N HCL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04058660
Source datasetuspto-grants-1977_11
ORD IDord-fab4856869f84449bf843e1ee6bcab46
Source noteuspto-grants-1977_11