HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095518Generated: October 31, 2026
Dimethyl Sulfoxide → 3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl ester
https://huagongshe.com/reaction/2095518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl ester | HCID 67074007 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl ester | HCID 86652690 | — |
Reaction Steps
To a solution of 0.55 ml (6.3 mmol) of oxalyl chloride in 21 ml CH2Cl2 at −50 to −60° C. was added a solution of 0.93 ml (13.1 mmol) dimethylsulfoxide in 7 ml of CH2Cl2 within 20 min. The solution was stirred for 5 min, then a solution of 2.10 g (5.5 mmol) of 3-[(3-chloro-4-trifluoromethoxy-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl ester in 14 ml CH2Cl2 was added within 20 min. The mixture was stirred for 15 min and 3.81 ml (27.4 mmol) of triethylamine were added within 20 min. The suspension was stirred for 3 h and slowly warmed to −5° C. The reaction was neutralized with cold aqueous 10% KH2PO4 (adjusted with solid KH2PO4 to pH 4-5) and extracted with EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3 (freshly prepared), aqueous 10% NaCl, dried over Na2SO4 evaporated to yield 2.21 g (quantitative) of the title compound as yellow oil. MS: 381 (M+, Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08445674B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-9bdc09a5c69d47f0b58fb9d763f4e6df |
|---|
| Source note | uspto-grants-2013_05 |
|---|