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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597705Generated: October 30, 2026

Bromoacetyl bromide → 1-(Bromoacetyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/597705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
SolventBenzeneHCID 241—
Product1-(Bromoacetyl)-1,2,3,4-tetrahydroquinolineHCID 583814—

Reaction Steps

To a stirred solution of 20.2 g. of bromoacetyl bromide in 150 ml. of benzene is added dropwise over 30 minutes, 26.6 g. of 1,2,3,4-tetrahydroquinoline dissolved in 35 ml. of benzene. The reaction mixture is then stirred at room temperature for 18 hours, after which time the precipitate is filtered off. The resultant filtrate is washed successively with 1N HCL solution and with a saturated sodium chloride solution, dried, and the solvent removed under reduced pressure to yield 1-(bromoacetyl)-1,2,3,4-tetrahydroquinoline, b.p. 70°-80° C. (at 0.1 mm. Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04015005
Source datasetuspto-grants-1977_03
ORD IDord-ce6c420f2dd44392ad412c7d98e22342
Source noteuspto-grants-1977_03