HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Benzyl 4-(3-hydroxypropyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (Phenylmethyl) 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate | HCID 12674069 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 4-(3-hydroxypropyl)piperidine-1-carboxylate | HCID 14989193 | 61.6% |
Reaction Steps
To a stirred and cooled (ice bath, 10° C.) mixture of 3.4 parts of sodium tetrahydroborate and 188 parts of N,N-dimethylformamide were added dropwise 28 parts of (phenylmethyl) 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate (exothermic reaction, the temperature rose to 38° C.). Upon completion addition, the reaction mixture was stirred over weekend at room temperature. The reaction mixture was poured into water and the product was extracted with methylbenzene. The extract was dried, filtered and evaporated, yielding 15.4 parts (61.6%) of (phenylmethyl) 4-(3-hydroxypropyl)-1-piperidinecarboxylate as a residue (int. 35).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05231184 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-e5fbd2d085b84ab38a8b8d7eecf78437 |
| Source note | uspto-grants-1993_07 |