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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174863Generated: October 30, 2026

Isopropyl Acetate → (2r,4s)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid potassium salt

https://huagongshe.com/reaction/2174863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl AcetateHCID 7915—
ReactantHCID 66957978HCID 66957978—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product(2r,4s)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid potassium saltHCID 66957981—

Reaction Steps

100 mg (R)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acid potassium salt (2-a, R1=Boc, R2=H, R3=CO2K) (prepared according to procedure in Example 42) is added to isopropyl acetate (1 ml). 10% Palladium on carbon (10 mg, 50% water wet, Degussa type E101 NE/W) is then added. Hydrogen gas at ambient pressure is applied to the mixture. The mixture is stirred at ambient temperature and pressure overnight. The mixture is then filtered over Celite and washed with isopropyl acetate (2×1 ml). The mixture is then concentrated in vacuo to give (2R,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid potassium salt (1-a, R1=Boc, R2=H, R3=CO2K) and (2S,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid potassium salt (1-b, R1=Boc, R2=H, R3=CO2K). Spectroscopic data as in Example 42, Method 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061973B2
Source datasetuspto-grants-2015_06
ORD IDord-815f4df07caa4b8a8b3d2d49f40314e5
Source noteuspto-grants-2015_06