HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (s)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | HCID 178420793 | HCID 178420793 | — |
| Product | (s)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanol | HCID 44249051 | — |
Reaction Steps
(S)-Epichlorohydrin (48.0 mL, 0.612 mol) was added to a stirred solution of piperazine N-methylsulfonamide (87.3 g, 0.532 mol) in ethanol (1.33 L) at room temperature. The reaction mixture was stirred for 18 h and the white solid precipitate which formed was collected by filtration and washed with ethanol to provide the title intermediate (107.7 g) as a white solid which was used without further purification. (m/z): [M+H]+ calcd for C8H17ClN2O3S, 257.07. found, 257.2. 1H-NMR (DMSO): δ(ppm) 5.09 (d, 1H), 3.84 (m, 1H), 3.65 (dd, 1H), 3.55 (dd, 1H), 3.09 (m, 4H), 2.37 (dd, 1H), 2.86 (s, 3H), 2.50-2.58 (m, 4H), 2.45 (dd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772239B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-e96facf17997467ea63384cc0bcb3082 |
| Source note | uspto-grants-2010_08 |