HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194983Generated: October 26, 2026
Dimethylformamide → 3-Acetylsulfanyl-1-Boc-piperidine
https://huagongshe.com/reaction/2194983
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Boc-3-mesyloxypiperidine | HCID 568122 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Acetylsulfanyl-1-Boc-piperidine | HCID 54776238 | 47.1% |
Reaction Steps
2.7 l of dimetylformamide are placed in a reactor under inert atmosphere. 251.4 g of N-BOC-3(R,S)-methylsulfonyloxy-piperidine are added with warming. At an internal temperature of 50° C. 256.8 g of potassium thioacetate are added at once. After stirring for 90 min at 95° C. the reaction mixture is transferred into a reactor filled with 4 l of water. 4.2 l of petroleum ether are added. After vigorous stirring for 5 minutes the aqueous phase is removed. After readdition of water the pH is adjusted to >8 with sodium hydroxide. The organic phase is separated, washed with water and treated with active charcoal. The solution is evaporated to dryness. After flash chromatography on silica with petroleum ether, toluene, and ethyl acetate and concentration of the product containing solution crystallization occurs on cooling and 110 g of N-BOC-3(R,S)-acetylthio-piperidine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334389B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b4652405c8fb4bf2b7e1a60e4e17cb8d |
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| Source note | uspto-grants-2012_12 |
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