HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368058Generated: November 2, 2026
Water → tert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate
https://huagongshe.com/reaction/2368058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (S)-2-((tert-butoxycarbonyl)amino)propyl 4-methylbenzenesulfonate | HCID 13200311 | — |
| Reactant | HCID 178418642 | HCID 178418642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate | HCID 57517478 | 20.7% |
Reaction Steps
To a suspension of sodium hydride (oil, 60%, 1.61 g) in DMF (50 mL) was added 4-hydroxypyridine (3.83 g) under ice-cooling. The reaction mixture was stirred for 30 min under ice-cooling, and (2S)-2-[(tert-butoxycarbonyl)amino]propyl 4-methylbenzenesulfonate (13.3 g) was added thereto in small portions under ice-cooling. The reaction mixture was stirred for 2 hr under ice-cooling, and at 60° C. for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08703758B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-48c3b04b55f444838f6783b89dbd48f3 |
|---|
| Source note | uspto-grants-2014_04 |
|---|