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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894382Generated: October 25, 2026

4-(Dimethylamino)Benzaldehyde → 2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penam

https://huagongshe.com/reaction/894382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
Reactant2,2-Dimethyl-3alpha-cyano-6alpha-bromopenamHCID 12944713—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70545653—
Product2,2-Dimethyl-3alpha-cyano-6beta-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70546902—

Reaction Steps

A solution of 100 mg 2,2-dimethyl-3α-cyano-6α-bromopenam in 40 ml dry tetrahydrofuran is stirred with 60 mg p-dimethylaminobenzaldehyde and 500 mg zinc for about 12 hours at room temperature. The reaction mixture is then diluted in ethyl acetate, washed with aqueous sodium chloride and dried over anhydrous sodium sulfate. Chromatography of the mixture on silica gel affords, in 11:1 ratio, 2,2-dimethyl-3α-cyano-6α-(p-dimethylamino-α-hydroxybenzyl)penam and 2,2-dimethyl-3α-cyano-6β-(p-dimethylamino-α-hydroxybenzyl)penam. The 6α-compound has the following formula: ##STR39##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04283531
Source datasetuspto-grants-1981_08
ORD IDord-778f6392483544c6bae51ae7e02cf154
Source noteuspto-grants-1981_08