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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034500Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 131718419, compound

https://huagongshe.com/reaction/1034500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 22851794HCID 22851794—
SolventPyridineHCID 1049—
ProductHCID 131718419HCID 13171841960.5%

Reaction Steps

To a solution of (2S,4R)-1-p-methoxybenzyloxycarbonyl-4-hydroxypyrrolidine-2-methanol (64 g: 227.6 mmole) in pyridine (350 ml), p-toluenesulfonyl chloride (48 g) is added. The mixture is stirred at room temperature for 4 hours. The reaction mixture is poured into ice water and extracted with ethyl acetate. The extract is successively washed with water, dilute hydrochloric acid and aqueous sodium hydrogen carbonate, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography to give (2S,4R)-1-p-methoxybenzyloxycarbonyl-4-hydroxypyrrolidine-2-methanol p-toluenesulfonate (60 g). NMR δ(CDCl3) ppm: 2.0 to 2.4(m, 2H), 2.44(s, 3H), 3.3 to 3.7(m, 2H), 3.82(s, 3H), 3.9 to 4.6(m, 4H), 4.8 to 5.1(m, 2H), 6.88(d, J=8.6 Hz, 2H),7.2 to 7.4(m, 4H), 7.6 to 7.8(m, 2 H). IR ν (CHCl3) cm-1 : 3446, 1693.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317016
Source datasetuspto-grants-1994_05
ORD IDord-0b0c65670c0d4d33b077436a373c8a17
Source noteuspto-grants-1994_05