HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 59655846, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Water ethylacetate | HCID 22728543 | — |
| Reactant | HCID 59655900 | HCID 59655900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59655846 | HCID 59655846 | 73% |
Reaction Steps
A mixture of 3-aminomethyl-4-fluoro-1-trimethylstannylbenzene (505.4 mg, 1.76 mmol), Ac2O (215.3 μL, 2.28 mmol) and NEt3 (489 μL, 3.51 mmol) was stirred at room temperature in CH2Cl2 (18 mL). After 3 h, extractive EtOAc/H2O workup followed by flash chromatography (EtOAc/Hexanes, 40:60) provided the title compound (422 mg, 73%) as an oil. 1H NMR (DMSO, 400 MHz): 8.29 (br s, 1H), 7.41 (d, J=7.52 Hz, 1H), 7.45-7.30 (m, 1H), 7.14 (dd, J=10.9, 8.2 Hz, 1H), 4.27 (d, J=5.47 Hz, 2H), 1.85 (s, 3H), 0.26 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329668B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-67640b3cea5347a29a57d55941ce207d |
| Source note | uspto-grants-2008_02 |