Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299248Generated: October 30, 2026

Chloroacetyl chloride → HCID 18519345, compound

https://huagongshe.com/reaction/2299248

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 numberUS06495681B1
Source datasetuspto-grants-2002_12
ORD IDord-41d93ad3a3854e219e0d1342a144585c
Source noteuspto-grants-2002_12