HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-Butyl (6-(hydroxymethyl)pyrimidin-4-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tert-butyl (6-formylpyrimidin-4-yl)carbamate | HCID 23593604 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl (6-(hydroxymethyl)pyrimidin-4-yl)carbamate | HCID 72698493 | 31.1% |
Reaction Steps
To a stirred solution of the crude tert-butyl 6-formylpyrimidin-4-ylcarbamate (4.6 g, 0.020 mol) in MeOH (100 mL) was added sodium borohydride (0.74 g, 0.020 mol) in four portions at room temperature. After addition, the resulting mixture was stirred for 1 hour and then water (50 mL) was added. The solvent was removed under reduced pressure and the resulting aqueous residue was extracted with EtOAc (3×100 mL). The combined organic extract was washed with water (30 mL) and brine (30 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified via silica gel column chromatography, eluting with DCM/MeOH (30:1) to give the desired product (1.4 g, 30% yield). LCMS (ESI) m/z: 226.0 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697708B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-75da38fcc33842cf87c722e62493f4b2 |
| Source note | uspto-grants-2014_04 |