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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720397Generated: October 28, 2026

Phenacyl bromide → HCID 21892156, compound

https://huagongshe.com/reaction/720397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant5,6,7,8-TetrahydroquinolineHCID 66335—
ReactantHCID 13530044HCID 13530044—
SolventAcetonitrileHCID 6342—
ProductHCID 21892156HCID 21892156—

Reaction Steps

1-(Phenacyl)-5,6,7,8-tetrahydro-quinolinium bromide: The title compound was prepared from 2-bromo-1-phenyl-ethanone (507.7 mg, 2.55 mmol), 5,6,7,8-tetrahydro-quinoline (275 μL, 2.13 mmol) and acetonitrile (4.2 mL), similar to Example 1a, and yielded 694 mg (98%) as a light tan solid. 1H NMR (DMSO-d6): 8.80 (d, J=6.05 Hz, 1H), 8.45 (d, J=7.70 Hz, 1H), 8.11 (d, J=7.97 Hz, 2H), 8.00 (dd, J=7.69, 6.31 Hz, 1H), 7.82 (t, J=7.42 Hz, 1H), 7.68 (t, J=7.56 Hz, 1H), 6.52 (s, 2H), 3.02 (t, J=6.18 Hz, 2H), 2.92 (t, J=6.18 Hz, 2H), 1.85 (m, 2H), 1.77 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135480B2
Source datasetuspto-grants-2006_11
ORD IDord-b833b566ba614368a348aa96f9843ed0
Source noteuspto-grants-2006_11