HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076521Generated: October 30, 2026
N,N-Dimethylaniline → 6-Aminopenicillanic acid
https://huagongshe.com/reaction/1076521
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Ethylmethylphosphinic chloride | HCID 83238 | — |
| Reactant | Phosphorus | HCID 5462309 | — |
| Reactant | CID 66586213 | HCID 66586213 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Aminopenicillanic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957771 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-d9eed68a41954cf6804ff4749aea622a |
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| Source note | uspto-grants-1976_05 |
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