HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070548Generated: October 30, 2026
Triethylamine → 6-Methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl ester
https://huagongshe.com/reaction/2070548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Hydroxy-spiro[4.5]decane-7-carboxylic acid methyl ester | HCID 57771536 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl ester | HCID 57771563 | — |
Reaction Steps
To a solution of 6-hydroxy-spiro[4.5]decane-7-carboxylic acid methyl ester (10.1 g) obtained in Step 3 and triethylamine (19.9 mL) in chloroform (100 mL) was added dropwise methanesulfonyl chloride (5.2 mL) under ice-cooling, followed by stirring the reaction mixture at room temperature for 2 hours. Then, after addition of triethylamine (10 mL), the reaction mixture was stirred at room temperature for 30 minutes. After ice-cooling, ice-cold water (30 mL) and saturated aqueous sodium bicarbonate solution (50 mL) were added to the reaction mixture, followed by separation of the organic layer. The organic layer was washed with saturated brine, dried and concentrated to give a crude 6-methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl ester (22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299296B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-de9ee4fd15044adaa9116f8386be08c0 |
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| Source note | uspto-grants-2012_10 |
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