HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27136Generated: October 28, 2026
Sodium Hydroxide → HCID 178503834, compound
https://huagongshe.com/reaction/27136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Methylsulfanyl)acetyl chloride | HCID 11126256 | — |
| Reactant | 7-Amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid | HCID 178513909 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178503834 | HCID 178503834 | — |
Reaction Steps
To a stirred, cooled (-20°) solution of 10.2 g. (0.026 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 220 ml. of 3% sodium bicarbonate and 220 ml. of acetone is dropwise added a solution of 3.66 g. (0.029 mol.) of methylmercaptoacetyl chloride in 52 ml. of acetone, during which time the pH of the reaction mixture is maintained at 8.0 by addition of 10% sodium hydroxide. After addition the reaction mixture is stirred an additional 20 minutes at -15°, then is warmed to 25° and extracted with ether. The remaining aqueous phase is cooled, 250 ml. of ethyl acetate is added and the slurry is acidified with 3N hydrochloric acid. The layers are separated and the aqueous phase is extracted twice more with ethyl acetate. The combined extracts are dried (MgSO4) and evaporated to dryness to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04220644 |
|---|
| Source dataset | uspto-grants-1980_09 |
|---|
| ORD ID | ord-17aafc8a8d6d4384bb37bf8ee908d9a0 |
|---|
| Source note | uspto-grants-1980_09 |
|---|