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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017550Generated: October 30, 2026

1,2-Dichloroethane → HCID 53780410, compound

https://huagongshe.com/reaction/1017550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzyl AlcoholHCID 244—
ReactantHCID 15172357HCID 15172357—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 53780410HCID 5378041077.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

The product from Step B (5.4 g, 26.2 mmol) was taken up in DCM (50 mL) with stirring and cooled to 0° C. EDC (6.0 g, 31.4 mmol) and DMAP (164 mg, 1.31 mmol) were added followed by benzyl alcohol (2.4 mL, 23.6 mmol). The resulting solution was stirred at room temperature overnight with the exclusion of moisture. The reaction was diluted with DCM and washed successively with 1 M HCl, water, 5% Na2CO3 solution, brine and dried, filtered and evaporated to give a dark oil. This was purified by silica gel column chromatography eluting with hexane/ethyl acetate 1:1 to give the product as an orange oil (5.98 g, 70%). 1H-NMR δ (CDCl3) 7.38-7.17 (10H, m); 5.11 (2H, s), 4.08 (1H, m), 2.96 (2H, d, J=6.4 Hz), 2.64 (2H, d, J=6.4 Hz) and 2.27 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479502B1
Source datasetuspto-grants-2002_11
ORD IDord-54e0dfff6d79403cb7d556d4c8efbf07
Source noteuspto-grants-2002_11