HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (3-Bromo-2-ethylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57506022 | HCID 57506022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromo-2-ethylphenyl)methanol | HCID 58494037 | 59.4% |
Reaction Steps
To a solution of 3-bromo-2-ethylbenzaldehyde (5 g, 23.47 mmol) in Methanol (50 mL) was added NaBH4 (1.776 g, 46.9 mmol) at 0° C. The reaction solution was stirred at room temperature for 2 hours. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate, washed with water, dried over sodium sulphate, concentrated and purified by ISCO column chromatography to afford (3-bromo-2-ethylphenyl)methanol (D133) (3 g) as an oil. MS (ES): C9H11BrO requires 213.99. found 197.0 (M+H+-18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389508B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-52b5562d3a404dc19a1d7688650a783c |
| Source note | uspto-grants-2013_03 |