HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17004Generated: October 29, 2026
Acetonitrile → (R)-2-benzyloxycarbonyl-amino-3-(1-methylcyclopentyl)propionic acid methyl ester
https://huagongshe.com/reaction/17004
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Benzyloxycarbonylamino-3-(1-methylcyclopentyl)propionic acid methyl ester | HCID 67391470 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | (R)-2-benzyloxycarbonyl-amino-3-(1-methylcyclopentyl)propionic acid methyl ester | HCID 67547823 | — |
Reaction Steps
2-Benzyloxycarbonylamino-3-(1-methylcyclopentyl)-propionic acid methyl ester (7.6 g, 23.8 mmol) was dissolved in a mixture of acetonitrile (82 mL) and 0.2 M aqueous NaHCO3 (158 mL) and Alcalase 2.4 L (1.1 mL) was added and the reaction mixture was stirred vigorously for 8 h. The reaction mixture was then evaporated at 30° C. to remove acetonitrile, and the aqueous residue was washed with ether. The ethereal layer was concentrated to yield (R)-2-benzyloxycarbonyl-amino-3-(1-methylcyclopentyl)propionic acid methyl ester (1.9 g). The aqueous phase was filtered with Celite®, the pH was adjusted to 3 with 6N HCl, and the solution was extracted with ethylacetate. The ethyl acetate layer was dried and evaporated to yield 2(8)-benzyloxycarbonylamino-3-(1-methylcyclopentyl)-propionic acid (1.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737300B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-f2c7c6fa73da48d7a2fdb897d04e1402 |
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| Source note | uspto-grants-2010_06 |
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