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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trimethylsilyl)oxazolidin-2-one | HCID 123514 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with N,N-diethylethanamine (1:1) | HCID 161127 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-Methylbenzene-1-sulfonic acid--N,N-dimethylaniline (1/1) | HCID 71353520 | — |
| Product | 7-Aminodeacetoxycephalosporanic acid | HCID 33498 | 347.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04058660 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-fab4856869f84449bf843e1ee6bcab46 |
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| Source note | uspto-grants-1977_11 |
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