HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511454Generated: October 26, 2026
Acetic Acid → (3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate
https://huagongshe.com/reaction/1511454
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Isocyanocyclopropane | HCID 2758008 | — |
| Reactant | (S)-tert-butyl 1-cyclobutyl-3-oxopropan-2-ylcarbamate | HCID 57893126 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate | HCID 57893114 | — |
Reaction Steps
To a solution of cyclopropylisonitrile (1.21 g, 18 mmol), (S)-tert-butyl 1-cyclobutyl-3-oxopropan-2-ylcarbamate (2.95 g, 13 mmol) in methylene chloride(20 mL), was added acetic acid (1.56 g, 26 mmol) at 0° C. After the addition was complete, the reaction mixture was allowed to warm to 25° C. and stirred for another 4 hours. The reaction mixture was diluted with 200 mL ethyl acetate and washed with a saturated solution of sodium bicarbonate, then brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the crude product was crystallized from 50 mL of ethyl acetate and hexane (v/v=1/1) to give (3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate (3.8 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211897B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-fb0f9205ee744d33ba0aa35a4009f1d5 |
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| Source note | uspto-grants-2012_07 |
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