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 | US07534794B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-d630742457bd4731bb09f6c254e43f8c |
| Source note | uspto-grants-2009_05 |