HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 5329910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 5329909 | HCID 5329909 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 5329910 | HCID 5329910 | 77.4% |
Reaction Steps
A suspension of Example 3 (0.088 g, 0.24 mmol) in THF (2 mL) was treated dropwise via syringe with acetyl chloride (0.017 mL, 0.24 mmol), stirred at room temperature overnight, quenched with water, cooled to 0° C., and filtered. The filter cake was dried to give 77 mg of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 2.17 (s, 3H); 2.28 (s, 3H); 4.55 (s, 2H); 6.80 (d, J=7.1 Hz, 1H); 7.16 (t, J=7.8 Hz, 1H); 7.24 (d, J=8.1 Hz, 1H); 7.31 (br s, 1H); 7.50 (d, J=8.8 Hz, 2H); 7.56 (d, J=8.8 Hz, 2H); 7.61 (d, J=8.5 Hz, 1H); 8.38 (d, J=8.1 Hz, 1H); 8.62 (s, 1H); 8.78 (s, 1H); 8.96 (s, 1H); 10.58 (s, 1H); MS (ESI(+)) m/e 415 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129260B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-e2fde09ae9e347b0983476843b8d4e2e |
| Source note | uspto-grants-2006_10 |