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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354645Generated: October 26, 2026

Acetyl chloride → 1-(4-Bromonaphthalen-1-yl)ethanone

https://huagongshe.com/reaction/354645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant1-BromonaphthaleneHCID 7001—
Reactant4-Bromo-1-naphthoic acidHCID 282591—
Product1-(4-Bromonaphthalen-1-yl)ethanoneHCID 230584—

Reaction Steps

The 4-bromo-1-naphthoic acid required as starting material according to the process according to the invention has already been described in the literature. It can, for example, be prepared in a simple manner by reacting 1-bromonaphthalene with acetyl chloride in a Friedel-Crafts reaction to give 4-bromo-1-acetylnaphthalene (see K. Dziewouski and L. Sternback, Bull. acad. polonaise A, 1931, 59 to 68, or T. L. Jacobs, S. Winstein, J. W. Ralls and J. H. Robson Journ. org. chem. 11 (1946), 27-33) and by oxidation of the latter compound with hypochlorite [see T. L. Jacobs et. al, see above, or N. J. Leonard and A. M. Hyson, J. Am. chem. soc. 71 (1949), 1963].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376214
Source datasetuspto-grants-1983_03
ORD IDord-4d1a97d3d84144b9ae7def1c9139d946
Source noteuspto-grants-1983_03