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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758534Generated: November 2, 2026

Acetonitrile → HCID 131712965, compound

https://huagongshe.com/reaction/1758534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzyl L-prolinateHCID 736155—
ReactantHCID 13101400HCID 13101400—
SolventEthyl AcetateHCID 8857—
ProductHCID 131712965HCID 131712965—

Reaction Steps

1,1-Carbonyldiimidazole (1.8 g., 0.011 mole) is added to a chilled (0°) solution of the product from part (c) (4.6 g., 0.011 mole) in 50 ml. of acetonitrile. The mixture is stirred for one hour at 0° and a solution of L-proline, benzyl ester (2.3 g., 0.011 mole) in 25 ml. of acetonitrile is added. The mixture is stirred at ambient temperature for 16 hours. The solvent is removed in vacuo. The residue is dissolved in 200 ml. of dichloromethane, washed with 5% potassium bisulfate, saturated sodium bicarbonate solution, brine, and dried (MgSO4). The solvent is removed in vacuo to give an oil residue of 6.5 g. Tlc, silica gel, ethyl acetate, shows a major spot at Rf 0.50 visualized with PMA. The residue is chromatographed on silica gel, eluted with dichloromethane/ethyl acetate (9:1) and (4:1) to give 5.4 g. of (±)-1-[(phenylmethoxy)[1-[(ethoxycarbonyl)amino]-3-phenylpropyl]phosphinyl]acetyl]-L-proline, phenylmethyl ester. Tlc shows a single spot at Rf 0.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374131
Source datasetuspto-grants-1983_02
ORD IDord-61f6072154524cd7aa47c55011450405
Source noteuspto-grants-1983_02