HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024659Generated: October 29, 2026
Ethyl Acetate → 1-(4-Tert-butylphenyl)-3-(3-hydroxypropyl)urea
https://huagongshe.com/reaction/1024659
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 1-Tert-butyl-4-isocyanatobenzene | HCID 2735695 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Tert-butylphenyl)-3-(3-hydroxypropyl)urea | HCID 53520686 | 110% |
Reaction Steps
A solution of 3-amino-1-propanol (0.180 mL, 2.36 mmol) in diethylether (15 mL) was cooled at 0° C. and treated dropwise with 1-tert-butyl-4-isocyanatobenzene (0.400 mL, 2.25 mmol). The reaction mixture was allowed to slowly warm to room temperature. After 16 h the reaction was found to be complete by TLC (100% ethyl acetate) The reaction mixture was diluted with 10 mL portions of Cl2Cl2 and Et2O and washed with 15 mL portions of H2O, 0.5N HCl and brine and dried over Na2SO4. The organic phase was filtered and concentrated to yield a colorless viscous oil which was dissolved in PhCH3, concentrated and placed under high vac overnight to yield the title compound (600 mg, 110%) as a colorless viscous oil: MS (ESI+) for C14H22N2O2 m/z 251.0 (M+H)+; (ESI−) for O14H22N2O2 m/z 249.3 (M−H)−; HPLC purity 98% (ret. time, 3.43 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722877B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-08cadd140b134521b62e29e07b78d74e |
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| Source note | uspto-grants-2014_05 |
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