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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751762Generated: October 31, 2026

1,2-Dichloroethane → HCID 59753381, compound

https://huagongshe.com/reaction/751762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPentafluorophenolHCID 13041—
ReactantHCID 86598032HCID 86598032—
SolventDichloromethaneHCID 6344—
ProductHCID 59753381HCID 59753381—

Reaction Conditions

Temperature-20 °C

Reaction Steps

3.95 g (5.41 mm ol) of the acid from example 25A and 3.98 g (21.65 mmol) of pentafluorophenol are dissolved in dichloromethane (13 ml) and cooled to −20° C. under argon. 1.14 g (5.95 mmol) of EDC are added, and the reaction mixture is stirred overnight with slow warming to RT. The reaction solution is concentrated to dryness and the residue is treated at 0° C. with 4N hydrogen chloride solution in dioxane (80 ml). The mixture is stirred for 3 h and the solvent is subsequently removed in vacuo. The residue is dissolved in dichloromethane (about 900 ml) and slowly added dropwise at RT to a vigorously stirred two-phase mixture of 1N aqueous sodium hydrogencarbonate solution (700 ml) and dichloromethane (1200 ml). The reaction mixture is stirred overnight. The phases are separated, the aqueous phase is extracted three times with dichloromethane and the combined organic phases are dried over sodium sulfate, filtered and concentrated to dryness. The residue (2.7 g of yellow hard foam) is purified by chromatography in 3 portions by means of preparative RP-HPLC using acetonitrile/water (gradient). 1.98 g (60% of th.) of the product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405201B2
Source datasetuspto-grants-2008_07
ORD IDord-9efe8c7fdb904e92a58444f8e299a5de
Source noteuspto-grants-2008_07