HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52201Generated: October 28, 2026
4-Toluenesulfonyl chloride → Ethyl acetate hexane
https://huagongshe.com/reaction/52201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | N-t-butyloxycarbonylnaphthylalaninol | HCID 70093534 | — |
| Reactant | HCID 131719947 | HCID 131719947 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl acetate hexane | HCID 21226206 | 82% |
Reaction Steps
Boc-Nal-CH2OTs. N-t-butyloxycarbonylnaphthylalaninol (3.71 g; 12.3 mmol) was dissolved in pyridine (15 ml) and the solution was cooled to -30° C. Tosyl chloride (2.36 g; 12.4 mmol) was added and the mixture was stirred to clearness at -30° C. and then put into the refrigerator overnight. Pyridine was removed in vacuo and the product was extracted with ether (4×30 ml). The organic layer was washed with 1N HCl (2×30 ml), H2O (1×30 ml), NaHCO3 5% (2×30 ml) and saturated NaCl (1×30 ml), then dried over Na2SO4, filtered and stripped to leave an oily residue which was crystallized from AcOEt/hexane (4.6 g; 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616605 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-fdeb293275524430832ed2aac56fc5ac |
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| Source note | uspto-grants-1997_04 |
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