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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860492Generated: November 1, 2026

HCID 21836543, compound → Benzyl 1,1-dioxo-1lambda~6~,4-thiazinane-4-carboxylate

https://huagongshe.com/reaction/860492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21836543HCID 21836543—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductBenzyl 1,1-dioxo-1lambda~6~,4-thiazinane-4-carboxylateHCID 2183649769.8%

Reaction Steps

To a solution of benzyl 4-thiomorpholinecarboxylate (4.8 g) in methanol (30 mL) and H2O (20 mL) was added oxone (16.2 g) under ice water cooling and the mixture was stirred at ambient temperature for 2 hours. The solution was evaporated in vacuo and partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The combined organic layer was washed with water and brine, dried over MgSO4 and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of hexane and EtOAc to give benzyl 4-thiomorpholinecarboxylate 1,1-dioxide as a colorless solid (3.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-7a1e27e969164e87bee0825720cfa23e
Source noteuspto-grants-2006_12