HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267259Generated: October 29, 2026
Methanesulfonyl chloride → HCID 13071123, compound
https://huagongshe.com/reaction/267259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 13071121 | HCID 13071121 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13071123 | HCID 13071123 | — |
Reaction Steps
A solution of 0.87 g (5 mmols) of 3-hydroxymethyl-2,4-dioxabicyclo[3,3,1]nonan-7-ol of the formula IIa in 5 ml of anhydrous pyridine is cooled to -20°C and, while stirring, treated with 1,1 ml (14,2 mmols) of methanesulphonyl chloride. The cooling bath is removed and the reaction mixture is added after 11/4 hours to 40 ml of a normal sodium bicarbonate solution. The resulting mixture is extracted successively with 40 ml of ethyl acetate and 40 ml of methylene chloride. The combined organic solutions are washed with 10 ml of sodium bicarbonate solution, dried over magnesium sulphate and concentrated in a water jet vacuum. The crude product is recrystallised from acetone/heptane and gives 7-methylsulphonyloxy-3-methylsulphonyloxymethyl-2,4-dioxabicyclo[3,3,1]nonane of the formula IIb ##SPC10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03941813 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-4a8a54ca9c3f47318ebb2e7190447813 |
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| Source note | uspto-grants-1976_03 |
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