HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (5-Tert-butyl-2-methoxy-3-nitrophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Tert-butyl-2-methoxy-3-nitrobenzaldehyde | HCID 58493990 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-Tert-butyl-2-methoxy-3-nitrophenyl)methanol | HCID 58493934 | — |
Reaction Steps
At approx. 10° C., 0.65 g sodium borohydride are added to a solution of 3.75 g 5-tert-butyl-2-methoxy-3-nitro-benzaldehyde in 15 ml dichloromethane and 15 ml of methanol. The solution is stirred for 2 h at ambient temperature and then evaporated down. The residue is combined with aqueous acetic acid and extracted with ethyl acetate. The combined extracts are washed with water and with saturated aqueous saline solution, dried (MgSO4) and evaporated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735579B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-96f2b8f7b82d4fcca41cf79b690c801e |
| Source note | uspto-grants-2014_05 |