Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625691Generated: November 1, 2026

Dichloromethane → HCID 58481132, compound

https://huagongshe.com/reaction/1625691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiketeneHCID 12661—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86658641HCID 86658641—
SolventEthyl AcetateHCID 8857—
ProductHCID 58481132HCID 58481132—

Reaction Steps

To (S)-methyl 6-amino-2-(2,2,2-trifluoroacetamido)hexanoate hydrochloride (0.943 g, 3.22 mmol), N,N-diisopropyl ethylamine (DIEA, 1.39 mL) and dichloromethane (DCM, 10 mL) in a 40 mL glass vial was added diketene (0.37 mL) under N2 atmosphere, and the reaction was stirred at ambient temperature for 16 hours. The reaction mixture was diluted with ethyl acetate (EtOA), washed successively with H2O, 1 N HCl, H2O, sat aq Na2CO3, and sat aq NaCl, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by a SiO2 flash chromatography, affording (S)-methyl-6-(3-oxobutanamido)-2-(2,2,2-trifluoroacetamido)hexanoate (TU3000-012) as a yellow oil. MS (ESI+): calcd. 341.12. found 341.10 (MH+). H-NMR (400 MHz, CDCl3):1.33 (2H, m), 1.55 (2H, m), 1.89 (2H, m), 2.259(3H, s), 3.31 (2H, m), 3.410 (2H, s), 3.783 (3H, s), 4.543 (1H, dt, J=4.4, 8.0 Hz). 7.091 (1H, br.s), 7.279 (1H, br.d, J=7.6 Hz). F-NMR (376 MHz, CDCl3): −75.609.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785151B2
Source datasetuspto-grants-2014_07
ORD IDord-5a1e908fcc2c4eedb0f6021ff91c7c51
Source noteuspto-grants-2014_07