HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519280Generated: October 25, 2026
Sodium borohydride → (2,6-Dibromo-4-fluorophenyl)methanol
https://huagongshe.com/reaction/519280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,6-Dibromo-4-fluorobenzaldehyde | HCID 44474666 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2,6-Dibromo-4-fluorophenyl)methanol | HCID 58043943 | 75% |
Reaction Steps
To a solution of 104k (20 g, 71 mmol) in EtOH (500 mL) was added NaBH4 (10 g, 284 mmol). The mixture was stirred at room temperature (10° C.) for 4 h and TLC showed the starting material had disappeared. The reaction was quenched by aqueous HCl solution (150 mL, 1M) and evaporated in vacuo until most of EtOH was distilled. The residue was extracted by ethyl acetate (500 mL×3). The organic layers were combined, dried with Na2SO4, and evaporated in vacuo. The residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate (from 50:1 to 20:1) to give 104l as a white solid (15g, 75%). MS: [M-OH]+ 267. 1H NMR (500 MHz, DMSO-d6) δ 7.68 (d, J=8.5, 2H), 5.23 (s, 1H), 4.71 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115152B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-ec5e5eb9257c4a00ae276016995db32f |
|---|
| Source note | uspto-grants-2015_08 |
|---|