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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501509Generated: October 30, 2026

Bromine → N-(4-Bromo-5,6,7,8-tetrahydronaphthalen-1-yl)-acetamide

https://huagongshe.com/reaction/501509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-Acetamido-5,6,7,8-tetrahydronaphthaleneHCID 232065—
SolventAcetic AcidHCID 176—
ProductN-(4-Bromo-5,6,7,8-tetrahydronaphthalen-1-yl)-acetamideHCID 1271030091.5%

Reaction Steps

To a solution of compound 2A (2 g, 11 mmol) in AcOH (15 mL) cooled at 0° C. was added a solution of bromine (1.69 mL, 33 mmol) in AcOH (1.2 mL) slowly so that the reaction temperature was maintained below 17° C. After addition, the reaction mixture was stirred at rt until all the starting material was consumed (˜4 h). The reaction mixture was then poured into ice/water and the resulting suspension filtered. The collected solid was washed with H2O until the filtrate pH=6-7, and dried in a vacuum oven at 50° C. overnight to yield compound 2B (2.7 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772267B2
Source datasetuspto-grants-2010_08
ORD IDord-3a26ffbc863f42c1805bbb2e89dc239b
Source noteuspto-grants-2010_08