HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651674Generated: November 1, 2026
Picolyl chloride hydrochloride → HCID 14621508, compound
https://huagongshe.com/reaction/1651674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Picolyl chloride hydrochloride | HCID 23392 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14621469 | HCID 14621469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14621508 | HCID 14621508 | 82.5% |
Reaction Steps
To a solution of (2R,4R,5S)-4-hydroxymethyl-5-[(Z) -6-methoxycarbonyl-2-hexenyl]-2-methyl-1,3-dioxane (272 mg) in N,N-dimethylformamide (10 ml) were added sodium hydride (80 mg, 60% in oil) and 2-picolyl chloride hydrochloride (110 mg) and the mixture was stirred at room temperature overnight. The reaction mixture was quenched with saturated aqueous ammonium chloride and the resulting solution was extracted with ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified with preparative thin layer chromatography with ethyl acetate as an eluent to give (2R,4R,5S)-5-[(Z)-6-methoxycarbonyl-2-hexenyl]-2-methyl -4-(2-pyridylmethoxymethyl)-1,3-dioxane (201 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929639 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-0cadf6e930004163bddfef78b5bcc65a |
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| Source note | uspto-grants-1990_05 |
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