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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Thiomorpholine, N-BOC protected | HCID 21949316 | — |
| Reactant | tert-Butoxycarbonyl dicarbonate | HCID 86600350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylate | HCID 21949260 | 91.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109219B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-78ccffa65a344032b23a9b0f65240757 |
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| Source note | uspto-grants-2006_09 |
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