HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 21841987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21841990 | HCID 21841990 | — |
| Product | HCID 21841987 | HCID 21841987 | — |
Reaction Steps
Into a solution of triphosgene (51.5 g, 174 mmol) in ethyl acetate (500 mL) heated to 75° C. was pumped a slurry of the title compound of Step B (15.57 g, 62 mmol) in ethyl acetate (100 mL) over 40 min. The mixture was held at 75° C. during the entire addition and then for an additional 2 h. The mixture was cooled to room temperature and stirred overnight. The reaction mixture was poured into saturated sodium bicarbonate solution and back-extracted with ethyl acetate. The combined organic phases were dried (MgSO4) and concentrated under reduced pressure to afford the title compound of Step C (14.59 g) as an off white solid. 1H NMR (CDCl3): δ 8.01 (dd,1H), 7.58 (d,1H), 7.50 (t,1H), 3.82 (s,3H), 3.56 (s,3H), 2.28 (s,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962436 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-b7549737707e4f8c8e4d77e0c8bce4b5 |
| Source note | uspto-grants-1999_10 |