HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 70043507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 70046065 | HCID 70046065 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70043507 | HCID 70043507 | 67.7% |
Reaction Steps
A solution of the indole 2 (29 g, 86 mmol), CH2Cl2 (450 mL), 1,8-diazobicyclo[5.4.0]undec-7-ene (38 mL, 0.26 mol), 4-dimethylaminopyridine (1.0 g, 8.5 mmol), and acetic anhydride (32 mL, 0.34 mol) was stirred for 1 week at ambient temperature. The reaction mixture was concentrated and then diluted with ether. The ether was then washed with H2O, 5% KHSO4 and brine, dried (MgSO4), and concentrated. Flash chromatography (silica, 5% ethyl acetate/hexanes) gave the acylated product 3 (27 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05321034 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-d4a4411eb58d4ed6a71f601e7b805da1 |
| Source note | uspto-grants-1994_06 |