HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034500Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 131718419, compound
https://huagongshe.com/reaction/1034500
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 22851794 | HCID 22851794 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131718419 | HCID 131718419 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05317016 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-0b0c65670c0d4d33b077436a373c8a17 |
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| Source note | uspto-grants-1994_05 |
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