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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076521Generated: October 30, 2026

N,N-Dimethylaniline → 6-Aminopenicillanic acid

https://huagongshe.com/reaction/1076521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantEthylmethylphosphinic chlorideHCID 83238—
ReactantPhosphorusHCID 5462309—
ReactantCID 66586213HCID 66586213—
Solvent1-ButanolHCID 263—
SolventDichloromethaneHCID 6344—
Product6-Aminopenicillanic acidHCID 11082—

Reaction Steps

To a suspension of 14.9 g of penicillin-G-potassium in 60 ml of absolute methylene chloride, 5.06 g (=40 mmols) of methylethylphosphinic acid chloride and 10 ml of dimethylaniline were added in the same manner as indicated in Example 1. The mixture was stirred for 1 hour and the solution of the mixed anhydride so prepared was converted at -5°C with 9.0 g (= 43 mmols) of phosphorus of pentachloride into the imidochloride. After addition of 60 ml of n-butanol and 2 ml of N,N-dimethylaniline, the mixture was stirred at -5°C for 30 minutes. 60 ml of ice water were added and the 6-aminopenicillanic acid was separated at pH 4. 6.47 g (= 76.4 % of the theory) of 6-aminopenicillanic acid were isolated in the form of colorless crystals having a melting point of 195°C (decomposition) which are identical with authentic 6-aminopenicillanic acid according to the IR-spectrum and the mixed melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957771
Source datasetuspto-grants-1976_05
ORD IDord-d9eed68a41954cf6804ff4749aea622a
Source noteuspto-grants-1976_05