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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250342Generated: October 30, 2026

Chloroacetyl chloride → HCID 18519345, compound

https://huagongshe.com/reaction/1250342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18519348HCID 18519348—
SolventDichloromethaneHCID 6344—
ProductHCID 18519345HCID 18519345—

Reaction Steps

Under a nitrogen atmosphere, 2,6-dimethyl-4-(octyloxy)-aniline (7.2 mmols) was dissolved in 50 mL dichloromethane. To this was added DIPEA (9.4 mmols). The reaction mixture was cooled in an ice bath, and chloroacetyl chloride (7.95 mmoles) dissolved in 50 mL dichloromethane was added by dropping funnel. After the addition was complete, the reaction was stirred at room until reaction was complete by TLC (approximately 0.5 hours). The reaction mixture was concentrated, and partitioned between ethyl acetate and water. The organic layer was washed with saturated NaHCO3(×2), brine, dried over MgSO4, and filtered (rinsing with ethyl acetate). The filtrate was concentrated to yield 2-chloro-N-(2,6-dimethyl-4-octyloxyphenyl)-acetamide as a white solid (1.21 grams; 51%). The product was characterized by NMR (DMSO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337423B1
Source datasetuspto-grants-2002_01
ORD IDord-e5154bb65eb54861b95f02576adc7d05
Source noteuspto-grants-2002_01