HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(3,4-Difluorophenyl)4-(ethoxycarbonylamino)-1-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Amino-3-(3,4-difluorophenyl)-1-butanol | HCID 22452637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(3,4-Difluorophenyl)4-(ethoxycarbonylamino)-1-butanol | HCID 22452677 | 88% |
Reaction Steps
Ethyl chloroformate (3.9 mL, 40.8 mmol) was added dropwise to a stirred cooled (−40° C.) solution of 4-amino-3-(3,4-difluorophenyl)-1-butanol (7.45 g, 37 mmol) and triethylamine (5.94 mL, 42.6 mmol) in DCM (180 mL). The solution was stirred at room temperature for 30 min and at room temperature overnight. The material was washed twice with 1N HCl, twice with saturated sodium bicarbonate; dried (Na2SO4), filtered and the solvent removed to provide the title compound (8.85 g, 88%) as a yellow oil. 1H-NMR (CDCl3) δ 1.18-1.23 (t, 3H, CH) 1.72-1.98 (m, 3H) 2.96-3.00 (m, 1H, CH) 3.24-3.29 (m, 1H, CH) 3.45-4.04 (m, 3H, CH), 4.06-4.14 (m, 2H, CH) 4.66 (br. s, 1H, OH or NH) 6.91-7.37 (m, 3H, ArH). MS m/z 274 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403601B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-9f2baada93884e98bedf46a8e507599e |
| Source note | uspto-grants-2002_06 |