Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496710Generated: October 31, 2026

1,2-Dichloroethane → HCID 59868529, compound

https://huagongshe.com/reaction/1496710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(3R)-3-(((tert-butoxy)carbonyl)amino)-4-phenylbutanoic acidHCID 7021561—
SolventPhosphoric AcidHCID 1004—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59868529HCID 598685296.3%

Reaction Steps

DIPEA (32.7 mL, 188 mmol) and EDC (15.4 g, 80.5 mmol) were added to a solution of (R)-3-t-butoxycarbonylamino-4-phenylbutyric acid (15.0 g, 53.7 mmol), HOBt (7.3 g, 53.7 mmol), and hydroxylamine hydrochloride (7.5 g, 107 mmol) in DMF (150 mL). The mixture was stirred at room temperature for 1 day and then concentrated in vacuo to yield a pale yellow oil. The oil was distributed between 5% THF in EtOAc and 1M phosphoric acid. The organic layer was collected and washed with 1M NaOH. The alkaline aqueous layer was then acidified using 1M phosphoric acid and extracted with EtOAc. The organic layer was evaporated and the residue was purified by silica gel chromatography (0-100% EtOAc in hexanes) to afford the title compound as a white solid (1.0 g, 3.4 mmol). MS m/z: [M+H+] calcd for C15H22N2O4, 295.16. found 295.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09198899B2
Source datasetuspto-grants-2015_12
ORD IDord-0c0c2a9bbb634a04a07a5b59ff48163e
Source noteuspto-grants-2015_12