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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861250Generated: November 2, 2026

1,2-Dichloroethane → HCID 19364751, compound

https://huagongshe.com/reaction/1861250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
Reactant(S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acidHCID 2734668—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 19364751HCID 1936475199%

Reaction Steps

To a suspension of H-pro-OBzl.HCl (2.00 g, 8.66 mmol) in CH2Cl2 (20 ml) was added DIEA (2.25 ml, 12.92 mmol) to give a colorless solution. Boc-tLeu-OH (1.95 g, 9.52 mmol), HOBT (1.76 g, 13.03 mmol) and EDC (2.49 g, 12.95 mmol) were added and the solution stirred under N2 at room temperature for 18 hours. Removed solvent in vacuo, dissolved in EtOAc and washed with H2O, 0.5N NaHSO4 (2×), saturated NaHCO3 (2×) and brine. Dried over anhydrous Na2SO4 and evaporated to give the title compound. (3.57 g, 99% yield). 1H-NMR (500 MHz, CDCl3) δ 0.99 (s, 9H), 1.40 (s, 9H), 1.88-2.33 (m, 4H), 3.58-3.90 (m, 2H), 4.21-4.35 (d, 1H), 4.53-4.66 (m, 1H), 5.04-5.38 (m, 3H), 7.14-7.42 (m, 5H). LC-MS (ES+) m/e=419.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531474B1
Source datasetuspto-grants-2003_03
ORD IDord-41250aad21614fd58ad1508b28f1ac9c
Source noteuspto-grants-2003_03