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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034496Generated: October 30, 2026

Sulfuric Acid → HCID 22851796, compound

https://huagongshe.com/reaction/1034496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium borohydrideHCID 4311764—
Reactant1,2-Pyrrolidinedicarboxylic acid, 4-[(methylsulfonyl)oxy]-, 1-[(4-methoxyphenyl)methyl] 2-methyl ester, (2S-trans)-HCID 10572279—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22851796HCID 2285179681.7%

Reaction Steps

To a solution of (2S,4R)-1-p-methoxybenzyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-carboxylic acid methyl ester (79.4 g: 205 mmole) in a mixture of tetrahydrofuran (200 ml) and ethanol (300 ml), sodium borohydride (14 g) is added in several portions under ice cooling. The mixture is stirred at room temperature for 4 hours. The reaction mixture is neutralized with conc. sulfuric acid, concentrated in vacuo to approximately a half volume, diluted with water, and extracted with ethyl acetate. The extract is successively washed with aqueous sodium hydrogen carbonate, water and brine, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography (toluene:ethyl acetate=1:2) to give (2S,4R)-1-p-methoxybenzyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanol (58.7 g). Yield: 81.7%. NMR δ(CDCl3) ppm: 1.8 to 2.2(m, 1H), 2.3 to 2.5(m, 1H), 3.01(s, 3H), 3.57 (d, J=4.4 Hz, 1H), 3.64(d, J=4.4 Hz, 1H), 3.81(s, 3H), 3.82 to 4.3(m,3H), 5.09(s, 2H), 5.21(br s, 1H), 6.89(d, J=8.8 Hz, 2H), 7.31(d, J=8.8 Hz,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317016
Source datasetuspto-grants-1994_05
ORD IDord-c3850c6883514f8eb7d12550b2a6110f
Source noteuspto-grants-1994_05