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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589065Generated: October 31, 2026

Hexane → HCID 57261056, compound

https://huagongshe.com/reaction/1589065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium HydroxideHCID 14923—
Reactant(S,R)-3-[[2-[(Acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]amino]-5-methylhexanoic acidHCID 57047065—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 57261056HCID 57261056—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of the (S,R) isomer product of Example 35 (1.0 g., 2.9 mmol.) in water maintained at 0° C. under argon was treated with ammonium hydroxide (5M solution, 10 mL, 50 mmol.) and stirred for 5 minutes. The reaction was quenched at 0° C. with 140 mL of 10% potassium bisulfate and then extracted with ethyl acetate (4×). The organic extracts were combined, dried (MgSO4), filtered, and concentrated in vacuo to yield 1.0 g. of yellow solid. The crude reaction product was flash chromatographed on 200 mL of silica gel eluting with hexane:ethyl acetate (2:1) to isolate 0.61 g. of the title (S,R) isomer product as a white solid, m.p. 155°-156° C., TLC Rf =0.19 (hexane:ethyl acetate:acetic acid, 100:100:1). [α]D =-55.5° (c=0.89, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05223516
Source datasetuspto-grants-1993_06
ORD IDord-760d7ac0e07742d09f720a98a90b26d5
Source noteuspto-grants-1993_06