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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702709Generated: October 30, 2026

Acetic Acid → HCID 131712810, compound

https://huagongshe.com/reaction/1702709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrabutylammonium borohydrideHCID 169536—
ReactantHCID 13065655HCID 13065655—
SolventDichloromethaneHCID 6344—
ProductHCID 131712810HCID 131712810—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Pivaloyloxymethyl 2-diazo-3-methyl-1-betaoxoceph-3-em-4-carboxylate (150 mg., 0.42 mmoles) was converted to a methylene chloride solution of pivaloyloxymethyl 2-methyl-1-oxocarbapen-2-em-3-carboxylate by the method of Example 1. Without isolation, and while continuing to maintain the temperature at -78° C., tetrabutylammonium borohydride (26.4 mg., 0.092 mmole) was added and the mixture stirred for 30 minutes. The reaction was quenched with acetic acid (0.58 equivalent), extracted twice with aqueous buffer (pH 7), dried over anhydrous sodium sulfate and filtered to yield a methylene chloride solution of pivaloyloxymethyl 1-hydroxy-2-methylcarbapen-2-em-3-carboxylate [ir (CH2Cl2) 1780, 1745 cm-1 ; Rf 0.25, (4:1 chloroform:ethyl acetate)]. If desired, this product is further isolated by evaporation in vacuo, keeping the temperature as low as possible to minimize degradation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348264
Source datasetuspto-grants-1982_09
ORD IDord-c76264ab8bbd444eb387af8b8f5cffc7
Source noteuspto-grants-1982_09