HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266872Generated: October 31, 2026
2-Methylbenzenesulfonic acid → HCID 86616136, compound
https://huagongshe.com/reaction/2266872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 68428479 | HCID 68428479 | — |
| Reactant | 769169-13-3 | HCID 86594487 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86616136 | HCID 86616136 | — |
Reaction Steps
A suspension of N-[(1S,2R)-1-cyano-4,4,4-trifluoro-2-methylbutyl]-4-methylbenzenesulfinamide (2.34 g, 7.69 mmol) in concentrated hydrochloric acid (75 mL) was heated to reflux for 18.5 h. After cooling to 25° C., the reaction mixture was washed with diethyl ether several times. The aqueous layer was concentrated to give a mixture of 5,5,5-trifluoro-L-alloisoleucine, NH4Cl, and toluenesulfonic acid (2.35 g). The crude amino acid was used in the next step without further purification. Mass spectrum (−ESI): 309 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858658B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-2e3353d20580430ebcc507cf4e50c8a6 |
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| Source note | uspto-grants-2010_12 |
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