HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (S)-4-(acetylamino)-5-fluoropentanoic acid, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-4-amino-5-fluoropentanoic acid methyl ester, hydrochloride | HCID 131714255 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (S)-4-(acetylamino)-5-fluoropentanoic acid, methyl ester | HCID 13477555 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
0.26 ml of triethylamine and 2 ml of glacial acetic acid were mixed with 0.34 g of 4. The mixture was cooled to 0° C. and 0.21 ml of acetic anhydride was added drop-by-drop to the stirred mixture. The mixture was allowed to warm to room temperature and stirred for 30 minutes. The solvents were evaporated under reduced pressure, the residue was triturated with a mixture of ethyl acetate and ether and filtered. The filtrate was eluted through a florisil pad, using ethyl acetate as eluent. The solvent was evaporated under reduced pressure to give 6, as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528028 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-a5d5670ede44466ea5141c263b072ce7 |
| Source note | uspto-grants-1985_07 |