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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339683Generated: October 29, 2026

Water → HCID 67233756, compound

https://huagongshe.com/reaction/339683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Bromo-4-fluoroanilineHCID 242873—
ReactantCrotonaldehydeHCID 447466—
CatalystZincchlorideHCID 3007855—
SolventHydrochloric AcidHCID 313—
ProductHCID 67233756HCID 6723375685%

Reaction Steps

2-Bromo-4-fluorobenzenamine (10 g, 52.6 mmol) was weighed into a round bottom flask, and dissolved in 40 mL of 6N HCl. The reaction mixture was then heated to reflux, followed by drop-wise addition of (E)-but-2-enal (4.578 mL, 55.3 mmol) mixed with 1.0 mL deionized water over 25 minutes. Following complete addition the reaction was heated at 100° C. for an additional 35 minutes, until all the 2-bromo-4-fluorobenzenamine had been consumed. The reaction was cooled to ambient temperature, followed by addition of 50 mL of Et2O. The reaction was stirred for 5 minutes followed by removal of Et2O by partitioning. The aqueous layer was replaced into the original reaction flask and ZnCl2 (3.586 g, 26.3 mmol) was then added in two portions followed by cooling to 0° C. over 30 minutes. The pH of the crude reaction mixture was then adjusted to pH=8.0 using concentrated NH4OH. The crude mixture was then extracted with Et2O, followed by ethyl acetate. The combined organics were then dried over Na2SO4, and then concentrated in vacuo, affording the desired product as a brown solid (10.7 g, 85% yield). MS APCI (+) m/z 240.2 and 242.2 (M+1 of each Br isotope) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895550B2
Source datasetuspto-grants-2014_11
ORD IDord-3491df3142bf40568ff5af6f4197cb42
Source noteuspto-grants-2014_11