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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419437Generated: November 2, 2026

Methyl iodide → HCID 13208311, compound

https://huagongshe.com/reaction/2419437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodiumHCID 5360545—
ReactantHCID 53898049HCID 53898049—
SolventEthanolHCID 702—
ProductHCID 13208311HCID 13208311—

Reaction Steps

Methyl iodide (71 g) is added to a solution of 1-(3-mercaptopropanoyl)-L-proline ethyl ester (115 g) and sodium (11.5 g) in ethanol (400 ml). The reaction is allowed to proceed overnight, the ethanol is removed in vacuo and the residue is dissolved in a mixture of ethyl acetate and water. The organic layer is dried and concentrated to dryness in vacuo. The resulting 1-(3-methylthiopropanoyl)-L-proline ethyl ester (98 g) is suspended in a mixture of methanol (200 ml) and 5 N sodium hydroxide (200 ml) and stirred at room temperature for five hours. The methanol is removed in vacuo, and the aqueous phase is extracted with ethyl acetate, acidified and reextracted with ethyl acetate. This last organic phase is washed with water, dried and concentrated to dryness to yield 1-(3-methylthiopropanoyl)-L-proline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105776
Source datasetuspto-grants-1978_08
ORD IDord-9bb96e51ba8e4c41b10343d0f5345690
Source noteuspto-grants-1978_08