HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 12223718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,2-Diacetoxy-3-chloropropane | HCID 95020 | — |
| Reactant | 10-Trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3-(2H)-dione | HCID 12223715 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12223718 | HCID 12223718 | — |
Reaction Steps
A mixture of 21.8 g. (0.112 mol.) of 3-chloro-1,2-diacetoxypropane, 28.0 g. (0.083 mol.) of 10-trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3(2H)-dione and 3.36 g. (0.080 mol.) of sodium hydride in 200 ml. of dry dimethylformamide was heated at 100°-110° for 40 hours in the presence of a catalytic amount of potassium iodide. The reaction mixture was filtered and the filtrate was evaporated to dryness under reduced pressure to give 2-(2,3-diacetoxypropyl)-10-trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3(2H)-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962438 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-574edea8d40a4d12ab0b28f5ebf5a28d |
| Source note | uspto-grants-1976_06 |