HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5-Trifluorobenzaldehyde → 3,4,5-Trifluorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5-Trifluorobenzaldehyde | HCID 2776954 | — |
| Reactant | water NaBH4 | HCID 131728255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4,5-Trifluorobenzyl alcohol | HCID 2777040 | 99.8% |
Reaction Steps
To a cooled (−5° C.) solution of 3,4,5-trifluorobenzaldehyde (7.0 g, 43.75 mmol) in a mixture (50 ml, 9:1) of THF and water NaBH4 (1.662 g, 43.75 mmol) was slowly added in portions over a period of 30 min. The reaction mixture was allowed to attain room temperature over a period of 2 h and carefully poured into ice-cold dil HCl (200 ml, IN). The oily layer was extracted into CH2Cl2 (250 ml) and the organic layer washed with water (200 ml), dried (MgSO4) and evaporated. The crude product (7.08 g, quantitative) obtained was taken forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829052B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-97c1f2314f3f464989316b7dcf70146e |
| Source note | uspto-grants-2014_09 |