HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842886Generated: November 1, 2026
Dimethyl Sulfide → (1-(2,3-dichlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine hydrochloride
https://huagongshe.com/reaction/1842886
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | 1-(2,3-dichlorophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carbonitrile | HCID 70816175 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-(2,3-dichlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine hydrochloride | HCID 86672141 | 27% |
Reaction Steps
To a stirred solution of 1-(2,3-dichlorophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carbonitrile (5.02 g, 16.46 mmol, 1.0 eq.) in THF (50 mL) was added BH3.S(CH3)2 (3.74 g, 49.38 mmol, 3.0 eq.) at 0° C. and heated to reflux for 1 h. The reaction mixture was cooled to 0° C. and quenched with 1N HCl and basified with 1N solution of NaOH to a pH of ˜10 and extracted with ethyl acetate (100 mL×2), dried (Na2SO4), the solvent evaporated to get a pale yellow oil. The oil was treated with ether HCl to get (1-(2,3-dichlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine hydrochloride (1.15, 27% yield over 3 steps) as a white solid (TLC system: CHCl3/MeOH (9:1), Rf 0.55).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946204B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-016ba02646af45368b0fb8e7a5b45290 |
|---|
| Source note | uspto-grants-2015_02 |
|---|