HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096197Generated: October 25, 2026
Dimethyl Sulfoxide → 3-[(3,4-Dichloro-phenyl)-(2-oxo-ethyl)-amino]-propionic Acid tert-butyl ester
https://huagongshe.com/reaction/1096197
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-[(3,4-Dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic Acid tert-butyl ester | HCID 66783234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(3,4-Dichloro-phenyl)-(2-oxo-ethyl)-amino]-propionic Acid tert-butyl ester | HCID 86638378 | 99.6% |
Reaction Steps
To a solution of 1.91 ml (21.77 mmol) of oxalyl chloride in 64 ml CH2Cl2 at −50 to −60° C. was added a solution of 3.22 ml (45.42 mmol) dimethylsulfoxide in 12 ml of CH2Cl2 within 20 min. The solution was stirred for 5 min, then a solution of 6.33 g (18.93 mmol) of 3-[(3,4-dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl ester in 43 ml CH2Cl2 was added within 20 min. The mixture was stirred for 15 min and 13.17 ml (94.63 mmol) of triethylamine were added within 20 min. The suspension was stirred for 3 h and slowly warmed to 0° C. The reaction was neutralized with cold aq. 10% KH2PO4 solution (adjusted with solid KH2PO4 to pH 4-5) and extracted with EtOAc (3×). The organic phases were washed with aq. 10% KH2PO4, solution sat. aq. NaHCO3 solution, aq. 10% NaCl solution, dried over Na2SO4 evaporated to yield 6.26 g (99.6%) of the title compound as orange oil. MS: 332.0 (MH+, 2Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-b889ae4f276446dea2c68f79a0ede20a |
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| Source note | uspto-grants-2012_03 |
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