HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307418Generated: October 25, 2026
Morpholine → [1-(3-Morpholin-4-yl-phenyl)ethyl]carbamic acid tert-butyl ester
https://huagongshe.com/reaction/2307418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Trifluoro-methanesulfonic acid 3-(1-tert-butoxycarbonylaminoethyl)phenyl ester | HCID 86589152 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [1-(3-Morpholin-4-yl-phenyl)ethyl]carbamic acid tert-butyl ester | HCID 69850623 | 153.6% |
Reaction Steps
A mixture of trifluoro-methanesulfonic acid 3-(1-tert-butoxycarbonylaminoethyl)phenyl ester (1.5 g, 4.08 mmol), morpholine (8 mL) Pd2(dba)3 (187 mg, 5 mol %), di-t-butyl-biphenylphosphine (243 mg, 20 mol %), potassium phosphate (1.21 g, 5.71 mmol) was stirred at 80° C. in a sealed tube for 10 hours. After cooling down, the reaction mixture was diluted with dichloromethane (50 mL) and washed with water (10 mL). The aqueous layer was extracted with dichloromethane (2×15 mL) and the combined organic layer was dried over magnesium sulfate and concentrated under vacuum. The crude product was purified by flash chromatography of Biotage with 30% ethyl acetate/hexanes to provide the title compound as a pale yellow solid (1.01 g, 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831080B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-bc23ea6c09be49498922e6282e198ea3 |
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| Source note | uspto-grants-2004_12 |
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