HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 13239942, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 604309 | HCID 604309 | — |
| Product | HCID 13239942 | HCID 13239942 | 97% |
Reaction Steps
2.1 g (6.6 mmol) of N-α-methylbenzyl-2-nitrobenzenesulfonamide was dissolved in 10 ml of epichlorohydrin, to which was gradually added at room temperature 0.35 g (7.3 mmol) of 50% sodium hydride, followed by agitating at room temperature for 30 minutes and reacting under reflux for 1 hour. The epichlorohydrin was distilled off under reduced pressure, water was added and extracted with ethyl acetate. The ethyl acetate phase was dried over anhydrous magnesium sulfate, concentrated, and purified by the silica gel chromatography to obtain the intended product (Compound No. 33). The yield was 97% and the nD26.5 value was 1.5572. The results of the elemental analysis are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04468245 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-4a1e3e3dbe90403daa02509876296502 |
| Source note | uspto-grants-1984_08 |