HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668538Generated: October 31, 2026
Dichloromethane → t-Butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate
https://huagongshe.com/reaction/1668538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate | HCID 58105232 | — |
| Solvent | Water | HCID 962 | — |
| Product | t-Butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate | HCID 58105230 | — |
Reaction Steps
To a 200 mL round-bottom flask, 50 mL of dichloromethane, 2.78 g of t-butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate and 2.0 g of diisopropylethylamine were added, and the mixture was stirred at ice temperature for 10 minutes. To the reaction mixture, 0.89 mL of methanesulfonyl chloride was added dropwise, and the mixture was stirred at room temperature for 3 hours. Water was added to the reaction mixture, and the mixture was partitioned. The organic layer was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and then the solvent was removed. The residue was purified by chromatography on silica gel (n-hexane-ethyl acetate=3:1) to give 2.28 g of t-butyl 5-(6-methane-sulfonyloxymethylpyridin-2-yl)pentanoate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989446B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-2baea6e96b8544059ce63e17b1a5ff9a |
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| Source note | uspto-grants-2011_08 |
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