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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537382Generated: October 30, 2026

1,2-Dichloroethane → HCID 86678255, compound

https://huagongshe.com/reaction/537382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzyl AlcoholHCID 244—
ReactantDichloromethaneHCID 6344—
ReactantHCID 86678254HCID 86678254—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
ProductHCID 86678255HCID 86678255—

Reaction Steps

A 2-dram vial containing a small stir bar was charged with (R)-2-(tert-butoxycarbonylamino)-3-ethyl-3-methylpentanoic acid (10b) (10 mg, 0.04 mmol), CH2Cl2 (1 mL), 4-dimethylaminopyridine (2 mg, 0.02 mmol, 0.5 equiv), benzyl alcohol (20 μL, 0.2 mmol, 5 equiv), and EDC (20 mg, 0.1 mmol, 2.5 equiv). The solution was stirred at room temperature for 3 h, and then diluted with 10 mL Et2O. The mixture was washed with water (2×10 mL), saturated aqueous NaHCO3 (10 mL), and brine (10 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel (7:1 hexanes/Et2O) and analyzed by chiral HPLC analysis: (AD-H, 1 mL/min, 5% IPA/hexanes, 210 nm): tR(major)=10.42 min, tR(minor)=12.87 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859812B2
Source datasetuspto-grants-2014_10
ORD IDord-5a2ad109942c44dbafbc214226484bfa
Source noteuspto-grants-2014_10