HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873594Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 178455320, compound
https://huagongshe.com/reaction/1873594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178455321 | HCID 178455321 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178455320 | HCID 178455320 | — |
Reaction Steps
16.4 g (129.47 mmol) oxalyl chloride are dissolved in 600 ml of dichloromethane and cooled to −78° C. 20.2 g (258.95 mmol) of dimethyl sulfoxide are then slowly added dropwise. The mixture is stirred for 5 min. After addition of a solution of 21.1 g (86.32 mmol) of the compound from Example 53A in 200 ml of dichloromethane the mixture is stirred at −78° C. for 1 h. 60 ml (431.58 mmol) of triethylamine are then slowly added dropwise. Over a period of one hour, the reaction mixture is then warmed to RT, and 500 ml of saturated aqueous sodium bicarbonate solution are then added. The phases are separated, the organic phase is dried over sodium sulfate and the solvent is removed on a rotary evaporator. The residue is purified chromatographically on silica gel 60 (mobile phase: gradient petroleum ether→petroleum ether/ethyl acetate 9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304412B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-1c4f3cd8115940508540c4a986214f97 |
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| Source note | uspto-grants-2012_11 |
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