Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895066Generated: October 30, 2026

Sodium Hydroxide → HCID 178503834, compound

https://huagongshe.com/reaction/895066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Methylsulfanyl)acetyl chlorideHCID 11126256—
Reactant7-Amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acidHCID 178513909—
SolventAcetoneHCID 180—
ProductHCID 178503834HCID 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 3 N 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04286089
Source datasetuspto-grants-1981_08
ORD IDord-ecd9eb697a9547548ea3a6373ebf991d
Source noteuspto-grants-1981_08