HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86686080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzyl 4-amino-5-hydroxy-azepane-1-carboxylic acid benzyl ester | HCID 86686081 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86686080 | HCID 86686080 | — |
Reaction Steps
3 mL acetic anhydride was added to 8.4 g benzyl 4-amino-5-hydroxy-azepane-1-carboxylic acid benzyl ester in 115 ml dichloromethane at 0° C. After 1 h at RT, saturated sodium bicarbonate was added. The phases were separated and the aqueous phase was extracted with dichloromethane. The combined organic phase was washed with brine, dried over sodium sulphate, filtered and concentrated. The residue was purified by chromatographie on silica gel (ethyl acetate/hexane 2:1) to yield 4.5 g of the desired product. (M+H)+: 307
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642774B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-6c5db16dab3b44c68f261948dac85555 |
| Source note | uspto-grants-2014_02 |