HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944100Generated: November 2, 2026
4-Toluenesulfonyl chloride → HCID 86668483, compound
https://huagongshe.com/reaction/1944100
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 52914724 | HCID 52914724 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86668483 | HCID 86668483 | 319.9% |
Reaction Steps
To a stirred solution of {(3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-2-hydroxymethyl-tetrahydro-pyran-2-yl}-methanol (Example 9, 500 mg, 0.70 mmol) in pyridine (15 mL) was added p-toluene sulfonyl chloride (670 mg, 0.21 mmol). After stirring for overnight at room temperature, reaction mixture was heated to 80° C. for another 18 h. The volatiles were evaporated, resulting residue was taken in ethyl acetate and washed with 1N HCl, brine, concentrated to furnish toluene-4-sulfonic acid (3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-2-hydroxymethyl-tetrahydro-pyran-2-ylmethyl ester (580 mg). The crude product was used as such for next step without purification which also contains small amount of bis-tosylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394772B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-240e1322ffa64302acd2fb0355bdeede |
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| Source note | uspto-grants-2013_03 |
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