HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474627Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 89442804, compound
https://huagongshe.com/reaction/1474627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 117762482 | HCID 117762482 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89442804 | HCID 89442804 | — |
Reaction Steps
Oxalyl chloride (0.086 mL, 1.01 mmol) was added to a solution of DMSO (0.14 mL, 2.0 mmol) in dry DCM (1 mL) at −78° C. under nitrogen atmosphere. The reaction mixture was stirred for 5 min. at the same temperature and then a solution of (2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(2-hydroxyethyl)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate (0.35 g, 0.6 mmol, prepared by following the procedure as described in WO2011070592), in dry DCM (3 mL) was added. The reaction mixture was stirred at the same temperature for 20 min. NEt3 (0.41 mL, 3.0 mmol) was added and the reaction mixture was allowed to come to r.t. Pet.ether (3 mL) was added to the reaction mixture and the solid was filtered. The filterate was concentrated in vacuo to afford the title compound, which was used as such in next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018249B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-64556c8f639146eda4cfd8ed3f13633b |
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| Source note | uspto-grants-2015_04 |
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