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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215532Generated: October 26, 2026

Sodium Thiosulfate → Tert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylate

https://huagongshe.com/reaction/2215532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantThiomorpholine, N-BOC protectedHCID 21949316—
Reactanttert-Butoxycarbonyl dicarbonateHCID 86600350—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylateHCID 2194926091.6%

Reaction Steps

tert-Butyl thiomorpholine-4-carboxylate (1.91 g, 9.42 mol) was dissolved in dichloromethane (50 ml); m-chloroperbenzoic acid (5.0 g, 19 mmol) was gradually added while cooled with ice bath, stirred, and under nitrogen atmosphere; and the reaction mixture was stirred at room temperature for 12 hours. After addition of a saturated aqueous solution of sodium thiosulfate, the reaction mixture was kept stirred for a while; and this was subjected to extraction with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Triethylamine (8.1 ml, 58 ml) were added to the obtained crystals; and the reaction mixture was stirred at room temperature. tert-Butoxycarbonyl dicarbonate (13.3 ml, 58 mmol) was added thereto; and the reaction mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure; and the obtained crystals were suspended with a solvent mixture of diethyl ether:ethanol=10:1, filtered off, washed with diethyl ether and dried under aeration to yield the title compound as colorless crystals (2.03 g, 8.63 mmol, 91.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109219B2
Source datasetuspto-grants-2006_09
ORD IDord-78ccffa65a344032b23a9b0f65240757
Source noteuspto-grants-2006_09