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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534833Generated: October 29, 2026

Hydrochloric Acid → HCID 66750915, compound

https://huagongshe.com/reaction/534833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 517510HCID 517510—
ReactantBis(2-chloroethyl)amine hydrochlorideHCID 522769—
SolventDiglymeHCID 8150—
SolventEthyl AcetateHCID 8857—
ProductHCID 66750915HCID 6675091514.7%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 2-tert-butyl-4-chloroaniline (Reference Example 19, 16.7 g, 90.8 mmol) and bis(2-chloroethyl)amine hydrochloride (17.8 g, 99.9 mmol) in diglyme (170 mL) was stirred at 170° C. for 3 days under nitrogen atmosphere. After this time, the reaction mixture was cooled to room temperature and partitioned between ethyl acetate and 1 M NaOH. The organic layer was washed with water, and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting brown oil was purified by flash column chromatography (NH-silica gel, 1:1-0:100 hexane/ethyl acetate, 10:1 ethyl acetate/MeOH) to provide an impure brown oil and a brown solid. The solid was dissolved in ethyl acetate and the solution was treated with 4 M HCl in ethyl acetate to give the title compound (2.17 g) as a brown solid. The impure brown oil was partitioned between ethyl acetate and 1 M HCl and the resulting white precipitate was collected by filtration, and washed with diethyl ether to give the title compound (2.98 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-23d3bd23071442aba80a20c0dece0b51
Source noteuspto-grants-2014_10