HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804560Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 57637086, compound
https://huagongshe.com/reaction/1804560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 57637044 | HCID 57637044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57637086 | HCID 57637086 | — |
Reaction Steps
10.81 ml (126.08 mmol) oxalyl chloride are placed in 300 ml dichloromethane and cooled to −70° C. 11.94 ml (168.11 mmol) dimethylsulphoxide are slowly added dropwise. The mixture is stirred for 0.1 hours, then 32.40 g (105.07 mmol) benzyl [2-(2-hydroxy-3-methyl-butylcarbamoyl)-ethyl]-carbamate in 70 ml dichloromethane are added. The mixture is stirred for 1 hour, then 62.48 ml (450.72 mmol) triethylamine are added dropwise. The reaction mixture is stirred for 1.5 hours at −70° C., then slowly allowed to come up to ambient temperature. It is diluted with dichloromethane and washed with 1 molar hydrochloric acid, saturated sodium carbonate solution, water and saturated sodium chloride solution. The organic phase is dried and evaporated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354418B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-f7189c1099284edcaa2d54c7b977bf68 |
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| Source note | uspto-grants-2013_01 |
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