HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 5-(tert-Butyl)-2-(hydroxymethyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-tert-Butyl-2-hydroxybenzaldehyde | HCID 13765272 | — |
| Reactant | Trifluoro-methanesulfonic acid 5-tert-butyl-2-formyl-phenyl ester | HCID 57424249 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(tert-Butyl)-2-(hydroxymethyl)phenol | HCID 19690241 | — |
Reaction Steps
A stirred, cooled (ice-bath) solution of a 1:1 mixture of trifluoro-methanesulfonic acid 5-tert-butyl-2-formyl-phenyl ester and 4-tert-butyl-2-hydroxy-benzaldehyde (Intermediate 105, 0.47 g) in methanol (8 mL) was treated with sodium borohydride (0.1 g, 2.64 mmol). After 1 h, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a residue that was subjected to flash column chromatography on silica gel (230-400 mesh) to afford the title product (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638648B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-1c77b02b420640d1bd0c0f5bc15bd75d |
| Source note | uspto-grants-2009_12 |