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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638165Generated: November 1, 2026

Methyl iodide → HCID 131713506, compound

https://huagongshe.com/reaction/638165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13603876HCID 13603876—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131713506HCID 131713506—

Reaction Steps

A solution of 1-[[[[ethoxy(4-phenylbutyl)phosphinyl]methyl]amino]carbonyl]-L-proline, phenylmethyl ester (2.43 g., 5 mmole) in dry tetrahydrofuran (15 ml.) is treated with 50% sodium hydride oil dispersion (0.24 g., 5 mmole) and stirred at room temperature for one hour. The mixture is then treated with methyl iodide (0.34 ml., 5.5 mmole) and stirred at room temperature for an additional 3 hours. The mixture is then partitioned between ethyl acetate--5% potassium bisulfate. The organic phase is washed successively with saturated sodium bicarbonate and saturated sodium chloride, dried (Na2SO4) and evaporated. The residue is purified by flash chromatograhy on silica eluting with acetone/dichloromethane (2:3) to give 1-[[methyl[[ethoxy(4-phenylbutyl)phosphinyl]methyl]amino]carbonyl]-L-proline, phenylmethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560681
Source datasetuspto-grants-1985_12
ORD IDord-793224bb6f4b49a794e7918a20de8cea
Source noteuspto-grants-1985_12