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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603344Generated: October 30, 2026

Chloroacetyl chloride → HCID 57952168, compound

https://huagongshe.com/reaction/603344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 57952164HCID 57952164—
SolventTolueneHCID 1140—
ProductHCID 57952168HCID 57952168—

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(2′,4′Dichloro-6′-methylphenyl)-4-ethylaniline (4.83 g as a mixture with the byproduct N,N-di-(4-ethylphenyl)-2′,4′-dichloro-6′-methylaniline) is dissolved in 4.18 g of chloro acetylchlorid and heated to 100° C. for 1.5 h. The mixture is cooled, diluted with toluene (50 ml) and extracted with aqu. sodium bicarbonate. The organic phase is evaporated to dryness and chromatographed on silica (75 g) eluting with toluene to afford unreacted N,N-di-(4-ethylphenyl)-2′,4′-dichloro-6′-methylaniline and N-(2′,4-dichloro-6′-methylphenyl)-N-chloroacetyl-4-ethylaniline (2.95 g). A crystallised sample melts at 83-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906677B2
Source datasetuspto-grants-2011_03
ORD IDord-0f7d2cc1ce57474d8094eb1386f50879
Source noteuspto-grants-2011_03