HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 90404382, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidine | HCID 10642851 | — |
| Reactant | (R)-tert-butyl 3-hydroxy-3-(3-hydroxyphenyl)propylcarbamate | HCID 90405310 | — |
| Product | HCID 90404382 | HCID 90404382 | — |
Reaction Steps
Alkylation of phenol (7, Intermediate I) with tert-butyl 4-((tosyloxy)methyl)piperidine-1-carboxylate following the method used in Example 11 gave (R)-tert-butyl 4-((3-(3-((tert-butoxycarbonyl)amino)-1-hydroxypropyl)phenoxy)methyl)piperidine-1-carboxylate as a colorless oil. Yield (0.70 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133154B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-e08da3f8991f4978abf05871255c21c3 |
| Source note | uspto-grants-2015_09 |