HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54376764, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 401453 | HCID 401453 | — |
| Solvent | Ethyl orthoformate | HCID 31214 | — |
| Product | HCID 54376764 | HCID 54376764 | 94% |
Reaction Steps
0.5 ml of acetic anhydride was added to 3.8 g (14.9 mmol) of 2-amino-3-carboethoxy-5-ethyl-4,5,6,7-tetrahydrothieno-[3,2-c]pyridine in 40 ml of triethyl orthoformate, and the mixture was boiled under nitrogen and at reflux for 1 h. After the mixture had been decanted off from the insoluble black coating on the flask walls, it was then evaporated right down at 80° C. on a rotary evaporator. 3.5 g (94%) of crude product were isolated as a dark oil which is sufficiently pure for further reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387912B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-c8ed0477ea2742c3bacbc56cc6c68854 |
| Source note | uspto-grants-2002_05 |