HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039599Generated: October 25, 2026
Triethylamine → 1-Ethoxycarbonyl-4-methyloxypiperidine
https://huagongshe.com/reaction/1039599
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Ethyl 4-hydroxypiperidine-1-carboxylate | HCID 96394 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Ethoxycarbonyl-4-methyloxypiperidine | HCID 45120191 | — |
Reaction Steps
1-ethoxycarbonyl-4-hydroxypiperidine (30.3 g) and triethylamine (23 g) were dissolved in ethyl acetate (182 mL) and the obtained mixture was cooled to 3° C. Methanesulfonyl chloride (22.05 g) was added thereto under stirring while taking caution such that the temperature did not exceed 20° C., and the mixture was continuously stirred under ice cooling for 1 hour. The obtained reaction mixture was washed with water (90 mL×3). The organic layer was isolated and concentrated to obtain a target compound as a light yellow oily substance. The yield amount was 43.09 g (98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552188B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-46653c60c6b244bfafb34f1aaeb28f08 |
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| Source note | uspto-grants-2013_10 |
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