HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → Hpr 611
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Methyl 2-oxo-5-chloro-3-benzothiazolineacetate | HCID 13040939 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Methoxide | HCID 10942334 | — |
| Product | Hpr 611 | HCID 3082453 | 80.8% |
Reaction Steps
4-Hydroxypiperidine (47.2 g) was added at room temperature to and dissolved in a methanolic sodium methoxide solution prepared from sodium metal (2.2 g) in dry methanol (100 ml). To the resultant solution was added methyl 5-chloro-2-oxo-3-benzothiazolineacetate (100 g), and the mixture was heated for 3 hours under reflux with stirring. The reaction mixture was left to cool, poured into ice water (500 ml) and stirred for 30 minutes. The precipitates were collected, washed with water and then dried to give 3-(4-hydroxypiperidino)carbonylmethyl-5-chloro-2-benzothiazolinone (102.5 g), which was recrystallized from 90% aqueous methanol to give colorless crystals, m.p. 180.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04131681 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-96b26f98857542468026d27821d2f913 |
| Source note | uspto-grants-1978_12 |