HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199769Generated: October 30, 2026
Ammonia → 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1199769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Amino-3-methoxymethyl-3-cephem-4-carboxylic acid | HCID 12833023 | — |
Reaction Steps
To 10 ml of nitromethane were added 3.0 g of 7-ACA, 10.0 g of zinc chloride and 3.9 g of a complex of boron trifluoride with methanol (boron trifluoride content: 51%). The mixture was heated at 60° C. for 20 min to advance a reaction. After completion of the reaction, the reaction mixture was cooled to 5° C. To the reaction mixture were added 30 ml of water and 5 ml of methanol. Then, the mixture was adjusted to pH 8.0 with 28% aqueous ammonia at a temperature of -5° C. The resulting precipitate was filtered off, and then washed with water. The filtrate was combined with the washings. The resulting mixture was adjusted to pH 3.5 with 36% hydrochloric acid to thereby form a precipitate. The precipitate was collected by filtration, and washed with 10 ml of cold water and, then, with 20 ml of cold methanol to obtain the desired product, namely 7-amino-3-methoxymethyl-3-cephem-4-carboxylic acid. The amount of the desired product was 1.4 g. The yield of the desired product was 52%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04902793 |
|---|
| Source dataset | uspto-grants-1990_02 |
|---|
| ORD ID | ord-bc48c4182d1e436a905c7f3ddc8ad6cc |
|---|
| Source note | uspto-grants-1990_02 |
|---|