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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThiomorpholine, N-BOC protectedHCID 21949316—
SolventWaterHCID 962—
ProductN-tert-butoxycarbonyl-5-oxo-4-thiapiperidineHCID 6734752297%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-40b3be5885594677ad86d2aec0f85ec0
Source noteuspto-grants-2011_08