HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670667Generated: October 31, 2026
4-Toluenesulfonyl chloride → HCID 71534086, compound
https://huagongshe.com/reaction/1670667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-dimethylformamide; methylsulfinylmethane | HCID 3013483 | — |
| Reactant | N-((Phenylmethoxy)carbonyl)-L-serine methyl ester | HCID 6999535 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71534086 | HCID 71534086 | 94% |
Reaction Steps
To a pre-cooled (−30° C.) solution of DMF:DMSO (1:1, 200 mL) under nitrogen was added TsCl (76.3 g, 0.4 mol) in small portions over 30 min. NOTE: This reaction is highly exotermic and careful temperature control is essential! The solution was stirred at −10° C. for 10 min, then again taken to −30° C. A solution of cbz-L-serine methyl ester (20.3 g, 0.08 mol, CAS 1676-81-9) in DMF was added dropwise, again with careful temperature control. After stirring for 10 min at −30° C. triethylamine (110 mL, 0.79 mol) was added and the reaction was slowly taken to 0° C. and kept at this temperature for 2 h. The reaction was quenched by addition of ice-cold water. The solution was extracted with 3×EtOAc, then the combined organic layer was washed extensively with brine and water. Drying and evaporation gave product as yellow oil (30 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994179B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-313ffdb48a8f4dffa8b7750654b8c4ea |
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| Source note | uspto-grants-2011_08 |
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