HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474614Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 89442841, compound
https://huagongshe.com/reaction/1474614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 117762492 | HCID 117762492 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89442841 | HCID 89442841 | — |
Reaction Steps
Oxalyl chloride (0.068 mL, 0.80 mmol) was added to a solution of DMSO (0.113 mL, 1.60 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 (2S,3S,4R,5S,6S)-2-(4-chloro-3-(4-(2-hydroxyethoxy)benzyl)phenyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triyl triacetate (220 mg, 0.403 mmol), in dry DCM (3 mL) was added. The reaction mixture was stirred at the same temperature for 1 h. NEt3 (0.334 mL, 2.40 mmol) was added and the reaction mixture was allowed to come to r.t. The crude compound was extracted with DCM (30 mL). The organic layer was separated, washed with water (15 mL). The combined organic layers were dried over Na2SO4 and 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-27386d14573344f6ae3dd08dc0f75881 |
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| Source note | uspto-grants-2015_04 |
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