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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259997Generated: October 30, 2026

Methanol → (2S, 4R)-4-hydroxy-N-(4-nitrobenzyloxycarbonyl)proline methyl ester

https://huagongshe.com/reaction/259997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactanttrans-4-Hydroxy-1-(4-nitrobenzyloxycarbonyl)-L-prolineHCID 10566895—
SolventDichloromethaneHCID 6344—
Product(2S, 4R)-4-hydroxy-N-(4-nitrobenzyloxycarbonyl)proline methyl esterHCID 18656014—

Reaction Steps

To a mixture of methanol (94.5 ml) and dichloromethane (945 ml) under ice cooling are dropwise added thionyl chloride (18.7 ml) and after 5 minutes stirring N-p-nitrobenzyloxycarbonyl-L-hydroxyproline (1: 72.4 g), and the mixture is stirred overnight at room temperature. The reaction mixture is concentrated in vacuum to give crude (2S,4R)-4-hydroxy-2-methoxycarbonyl-1-p-nitrobenzyloxycarbonylpyrrolidine (86.5 g) as pale yellow oil. This product can be used in the next step without further purification. IR ν (CHCl3) cm-1 : 3450, 1742, 1703, 1605. 1HNMR δ (CDCl3) ppm: 1.77(1H, s), 2.05 to 2.45(2H, m), 3.55 to 3.8(2H, m), 3.66, 3.76(3H, 2s), 4.49 to 4.62(2H, m), 5.06 to 5.35(2H, m), 7.43 to 7.56(2H, m), 8.22(2H, d, J=8.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523415
Source datasetuspto-grants-1996_06
ORD IDord-fbfed811205d4f8889b6dff5c84b4d57
Source noteuspto-grants-1996_06