HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256324Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 19029303, compound
https://huagongshe.com/reaction/2256324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19029306 | HCID 19029306 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19029303 | HCID 19029303 | 130.1% |
Reaction Steps
Oxalyl chloride (1.44 g) in CH2Cl2 (100 mL) was cooled to a -78° C. and treated with a solution of DMSO (1.84 g) in CH2Cl2 (20 mL) over 15 mins. This mixture was stirred for 15 minutes whereupon a CH2Cl2 (30 mL) solution of 3,4-Dichloro-beta-(2-hydroxyethyl)-N-[(3-fluoro-4-methoxyphenyl)methyl]benzenepropanamide (3.9 g) was added dropwise. The mixture was stirred for 30 minutes and then treated with a solution of Et3N (2.85 g) in CH2Cl2 (20 mL) and stirred for an additional 30 minutes at -78° C., then allowed to warm to ambient temperature. The reaction mixture was washed with water (100 mL), the organic fraction separated, dried over MgSO4, filtered and concentrated under reduced pressure to yield an oil (5.0 g). Silica gel chromatography eluting with 10% EtOAc/CH2Cl2 gave the title compound (3.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654316 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-903c37432ebb43c79770eada93baf5d0 |
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| Source note | uspto-grants-1997_08 |
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