HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494131Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 10380396, compound
https://huagongshe.com/reaction/1494131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 10335383 | HCID 10335383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10380396 | HCID 10380396 | — |
Reaction Steps
A solution of 1.62 mL (22.73 mmol) of dimethylsulfoxide in 60 mL dry methylene chloride is cooled to -78° C. and 1.44 mL (16.53 mmol) oxalyl chloride is added dropwise. The mixture is stirred 0.5 hour at -78° C. and a solution of 1.0 g (3.31 mmol) of 1-(3-pyridyl)-4-hydroxy-8-(2-tetrahydropyranyloxy)octane in 15 mL dry methylene chloride is added and the mixture is stirred for 10 minutes at -78° C. The mixture is warmed to -60° C. and maintained for 15 minutes at that temperature. The reaction is quenched by the addition of 6.9 mL triethylamine. The cold bath is removed and the reaction allowed to warm to room temperature. The reaction mixture is extracted with 150 mL methylene chloride and washed with saturated sodium bicarbonate solution. The organic phase is dried, filtered, concentrated and chromatographed using 3:2 ethyl acetate, hexane to yield 1-(3-pyridyl)-4-oxo-8-(2-tetrahydropyranyloxy)octane; NMR (CDCl3): delta 2.6 (t,2H), 2.4 (t,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025025 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-0f4b4ab6881c4b0a9d7e56a9f964ce5c |
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| Source note | uspto-grants-1991_06 |
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