HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22036362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (7-Amino-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanol | HCID 22036433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22036362 | HCID 22036362 | 46% |
Reaction Steps
Acetic anhydride (0.24 g, 2.4 mmol) was added to a stirred mixture of the title compound from Step 1 above (0.30 g, 1.66 mmol) and Et3N (0.70 g, 6.9 mmol) in CH2Cl2(30 mL). The reaction was stirred at room temperature for 15 h. More acetic anhydride (0.10 g, 1.0 mmol) was added and the mixture was stirred for a further 5 h at room temperature. The mixture was concentrated and the residue purified by chromatography on silica gel using EtOAc/isohexane (1:3 to 2:3) as eluent to give 170 mg (46%) of the title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071180B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-8b94bdbb09c74fa7bcbd2c63cdf905eb |
| Source note | uspto-grants-2006_07 |