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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266872Generated: October 31, 2026

2-Methylbenzenesulfonic acid → HCID 86616136, compound

https://huagongshe.com/reaction/2266872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acidHCID 6925—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 68428479HCID 68428479—
Reactant769169-13-3HCID 86594487—
SolventHydrochloric AcidHCID 313—
ProductHCID 86616136HCID 86616136—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858658B2
Source datasetuspto-grants-2010_12
ORD IDord-2e3353d20580430ebcc507cf4e50c8a6
Source noteuspto-grants-2010_12