HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-oxopiperidine-1-carboxylate → Tert-butyl 4-hydroxypiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | 100.8% |
Reaction Steps
1(tert-Butoxycarbonyl)-4-piperidone (5 g, 0.025 moles) was treated with sodium borohydride (1.89 g, 0.05 moles) as in the method of Example 37, Step 2 to give the title compound 5.07 g (100%); 1H NMR (CDCl3) inter alia 1.45 (9 H, s), 1.29-1.41 (2 H, m), 2.42-3.05 (2H, m), 3.75-3.99 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE039128E1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-58a1b15317f14ea3bfda143764b4b6ba |
| Source note | uspto-grants-2006_06 |