HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22161803, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22161767 | HCID 22161767 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22161803 | HCID 22161803 | — |
Reaction Steps
To a solution of 8-(t-butyldimethylsilyloxymethyl)-4-hydroxymethyl-1-ethyl-1,2,3,4-tetrahydroquinoline (1.98 g) in pyridine (5 ml), acetic anhydride was added dropwise with stirring under ice-cooling and the mixture was stirred for 2 hours at room temperature. Pyridine was distilled off under reduced pressure, and the resultant residue was extracted with dichloromethane. After washing with a saturated aqueous solution of copper sulfate and with water in this order, the mixture was dried and the solvent was distilled off under reduced pressure to give 8-t-butyldimethylsilyloxymethyl-4-acetyloxymethyl-1-ethyl-1,2,3,4-tetrahydroquinoline (2.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963566 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-eb43a212498e42418b51f5fbf2beee62 |
| Source note | uspto-grants-1990_10 |