HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960424Generated: October 31, 2026
Thiomorpholine → Tert-butyl [2-(benzylthio)-3-thiomorpholinopropyl]carbamate
https://huagongshe.com/reaction/1960424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Tert-butyl [2-(benzylthio)-3-oxopropyl]carbamate | HCID 59136000 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl [2-(benzylthio)-3-thiomorpholinopropyl]carbamate | HCID 59135685 | 91% |
Reaction Steps
To a solution of tert-butyl[2-(benzylthio)-3-oxopropyl]carbamate (820 mg) in tetrahydrofuran (30 mL) was added thiomorpholine (0.42 mL), and the mixture was stirred at room temperature for 1 hr. Sodium triacetoxyborohydride (1.76 g) was added to the reaction mixture under ice-cooling, and the mixture was stirred overnight at room temperature. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture under ice-cooling, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography to give the title compound (936 mg, yield 91%) as a colorless oil from a fraction eluted with is ethyl acetate-hexane (3:7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410087B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c77a687666bb48a39f774dadad5feb0d |
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| Source note | uspto-grants-2013_04 |
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