HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-chloro-1-methyl-1H-pyrazole-3-carbaldehyde → (4-chloro-1-methyl-1H-pyrazol-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-chloro-1-methyl-1H-pyrazole-3-carbaldehyde | HCID 2782153 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-chloro-1-methyl-1H-pyrazol-3-yl)methanol | HCID 55255171 | 90% |
Reaction Steps
To a solution of 4-chloro-1-methyl-1H-pyrazole-3-carbaldehyde (10.0 g, 69.2 mmol) in methanol (190 mL) was added sodium borohydride (3.93 g, 104 mmol) at 0° C. The mixture was stirred for 2 hours at room temperature and quenched with water. The solvent was evaporated, water was added, and the mixture was extracted 3 times with ethyl acetate. The combined organic phase was washed with brine and dried over sodium sulfate. After evaporation of the solvent, (4-chloro-1-methyl-1H-pyrazol-3-yl)methanol was obtained (9.04 g, 90% yield) and used in the next step without further purification; 1H NMR (500 MHz, DMSO-d6): δ 3.77 (s, 3H), 4.35 (d, J=5.5 Hz, 2H), 5.03 (t, J=5.5 Hz, 1H), 7.84 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040538B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-894f08e5df134d73b02bc8c178bb31c7 |
| Source note | uspto-grants-2015_05 |