HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266721Generated: October 29, 2026
Morpholine → (1-Methyl-2-morpholin-4-yl-ethyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/2266721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-tert-Butoxycarbonylaminopropyl methanesulfonate | HCID 14427184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-Methyl-2-morpholin-4-yl-ethyl)-carbamic acid tert-butyl ester | HCID 15326463 | 62% |
Reaction Steps
To a solution of methanesulfonic acid 2-tert-butoxycarbonylamino-propyl ester (23 mmol) in CH3CN (20 mL) was added morpholine (28 mmol) and K2CO3 (23 mmol) at room temperature. The reaction mixture was brought to 50° C. and kept at the same temperature overnight. The reaction mixture was cooled and solvent was removed under reduced pressure, and the residue was treated with CH2Cl2 (50 mL) and H2O (50 mL). The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organic layer was dried over Na2SO4. Solvent was removed under reduced pressure and the residue was purified by column chromatography (ethyl acetate) to afford (1-methyl-2-morpholin-4-yl-ethyl)-carbamic acid tert-butyl ester as viscous liquid, yield: 62%. MS (M+H)=245.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858654B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-97de1bcb9ea641fdbee97df1ed55b3cc |
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| Source note | uspto-grants-2010_12 |
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