HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480124Generated: October 26, 2026
Benzyl chloroformate → (1-Cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid benzyl ester
https://huagongshe.com/reaction/1480124
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-3-cyclopropyl-2-methyl-propionitrile | HCID 84716049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid benzyl ester | HCID 90204034 | 60% |
Reaction Steps
To a solution of 2-Amino-3-cyclopropyl-2-methyl-propionitrile (Example 66a, 5.01 g, 30.9 mmol) in dry THF (119 mL) was added DIEA (12.1 mL, 67.9 mmol) and benzyl carbonochloridate (CAN 501-53-1, 5.57 mL, 37.1 mmol). The reaction was stirred at 45° C. for 18 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethylacetate and extracted with an 1.0M aqueous solution of sodium bicarbonate. The organic layer was dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography eluting with a gradient of heptane/ethylacetate to yield the title compound (6.2, 60%) as a colorless oil. MS (ESI, m/z): 259.5 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409866B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-05123ffb9a4543f9a9175e88a87b33c5 |
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| Source note | uspto-grants-2016_08 |
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