HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Glycidol | HCID 11164 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-Tetrazole, 5-chloro-1-phenyl- | HCID 84262 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropane | HCID 12399823 | — |
Reaction Steps
Sodium hydride (11.9 g., 0.050 mole), washed free of mineral oil with hexane, was stirred in 1.8 l. of DMF at ice-water temperature while a solution of 72.3 g (0.40 mole) of 1-phenyl-5-chlorotetrazole and 29.6 g. (0.04 mole) of glycidol in 1.8 l. of DMF was added dropwise during 4 hours. The solution was allowed to stand at 25° overnight (16 hours), diluted with 12 l. of H2O and extracted with ethyl acetate. The extracts were washed with water, dried (Na2SO4), and evaporated to give 75.7 g. of product, m.p. 77°-81°. Recrystallization from MeOH-i-PrOH gave 55.8 g., m.p. 83°-84°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04252815 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-de7d0f7308d24e54b2ab6bd020617249 |
| Source note | uspto-grants-1981_02 |