HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75160Generated: October 29, 2026
Triethylamine → (S)-4-((tert-butyldiphenylsilyloxy)methyl)-1-(1-adamantylmethyl)imidazolidin-2-one
https://huagongshe.com/reaction/75160
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (S)-3-(tert-butyldiphenylsilyloxy)-N1-(1-adamantylmethyl)propane-1,2-diamine | HCID 68474186 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-4-((tert-butyldiphenylsilyloxy)methyl)-1-(1-adamantylmethyl)imidazolidin-2-one | HCID 68477189 | 156.3% |
Reaction Steps
A solution of triphosgene (124 mg, 0.42 mmol) in anhydrous CH2Cl2 (2 mL) was added slowly to a solution of (S)-3-(tert-butyldiphenylsilyloxy)-N1-(1-adamantylmethyl)propane-1,2-diamine (600 mg, 1.26 mmol) and triethylamine (140 mg, 1.4 mmol) in anhydrous CH2Cl2 (10 mL) at 0° C. The reaction mixture was stirred for another 1 h. The mixture was diluted with water and extracted with CH2Cl2 (50 mL). The organic layer was washed with 0.1 N aq HCl (2×20 mL) and brine (10 mL), dried over MgSO4 and concentrated to give a residue, which was purified by preparative TLC to provide (S)-4-((tert-butyldiphenylsilyloxy)methyl)-1-(1-adamantylmethyl)imidazolidin-2-one (330 mg, 52%). 1H NMR: (CDCl3, 400 MHz): δ=1.05 (s, 9H), 1.54 (s, 6H), 1.62-1.73 (m, 8H), 1.98 (s, 3H), 2.77 (m, 2H), 3.21 (m, 1H), 3.55 (t, 1H), 3.65 (m, 2H), 3.82 (m, 1H), 4.57 (s, 1H), 7.4 (m, 6H), 7.62 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835426B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a76ab5b3ff1a46f1917033eeac87f620 |
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| Source note | uspto-grants-2014_09 |
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