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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183910Generated: November 3, 2026

Acetyl chloride → HCID 86633185, compound

https://huagongshe.com/reaction/1183910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 86633184HCID 86633184—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
ProductHCID 86633185HCID 8663318583.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

Acetylchloride (1.36 mL, 19.1 mmol) was added slowly to a well-stirred solution of N-(3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-(2-methyl-2-nitropropoxy)phenyl)-2,2,2-trifluoroacetamide (889 mg, 1.91 mmol) in methanol (10 mL). Zinc dust (1.25 g, 19.1 mmol) was added in small portions, and the mixture was stirred at 55° C. After 2 h, the solvent was removed under reduced pressure, and residue was suspended in 1M HCl (10 mL) and covered with ethyl acetate. The mixture was cooled on an ice bath, and ammonium hydroxide was added until all precipitate dissolved. The layers were separated, and the aqueous layer was extracted with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried with sodium sulfate, filtered and evaporated to dryness to yield N-(4-(2-amino-2-methylpropoxy)-3-(4-bromo-2-methyl-2H-pyrazol-3-yl)phenyl)-2,2,2-trifluoroacetamide as a white powder (693 mg, 1.59 mmol, 83%). LCMS m/z (%)=437.3 (M+H 81Br 9.0%), 435.2 (M+H 79Br 14.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664258B2
Source datasetuspto-grants-2014_03
ORD IDord-5252df5ea25f40d697a745212e348a4b
Source noteuspto-grants-2014_03