HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676259Generated: October 30, 2026
Methanol → N-tert-butoxycarbonyl-5-oxo-4-thiapiperidine
https://huagongshe.com/reaction/1676259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thiomorpholine, N-BOC protected | HCID 21949316 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-tert-butoxycarbonyl-5-oxo-4-thiapiperidine | HCID 67347522 | 97% |
Reaction Steps
A mechanically-stirred mixture of tert-butyl thiomorpholine-4-carboxylate (243 g, 1.19 mol), MeOH (1.5 L), and H2O (1.5 L) was cooled to 0° C. Solid NaIO4 (280 g, 1.3 mol) was added in portions over a 2 hour period. For convenience, the suspension was stirred for 3 days at room temperature. The solids were filtered, washing with MeOH (3×500 mL). The filtrate was concentrated. Residual water was saturated with solid NaCl, and the aqueous phase was extracted with EtOAc (4×200 mL). The combined organic phases were dried (MgSO4), filtered, and concentrated to obtain the product (255 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003662B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-40b3be5885594677ad86d2aec0f85ec0 |
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| Source note | uspto-grants-2011_08 |
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