HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 44603856, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | HCID 12547487 | HCID 12547487 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 44603856 | HCID 44603856 | 99.7% |
Reaction Steps
TMSCN (0.3 mL, 2.25 mmol) was added to a mixture of compound 83 (120 mg, 0.75 mmol), acetone (0.33 mL, 4.5 mmol) and ZnCl2 (10 mg, 0.08 mmol) with stirring. The reaction mixture was stirred at room temperature for 1 h, and concentrated in vacuo. The residue was diluted with water, and extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to dryness to give compound 84 (170 mg, 99%) as a light yellow oil. The crude product was used directly for the next step without purification. 1H NMR (400 MHz, CDCl3) δ7.08 (d, 2H, J=8.1 Hz), 6.88 (d, 2H, J=8.1 Hz), 2.72 (t, 2H, J=7.4 Hz), 2.32 (t, 2H, J=7.4 Hz), 1.90-2.00 (m, 2H), 1.69 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216957B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-722c3f4dddc647888a5e5dc9ee542ff3 |
| Source note | uspto-grants-2015_12 |