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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44175Generated: October 26, 2026

2-Bromopropane → HCID 66911305, compound

https://huagongshe.com/reaction/44175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
Reactant6-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 14373281—
ReactantPotassium tert-butoxideHCID 23665647—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
ProductHCID 66911305HCID 6691130538.9%

Reaction Steps

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (750 mg, 3.32 mmol) in 20 ml dry DMF was added potassium tert-butylate (804 mg, 6.64 mmol). After the mixture was stirred for 30 min at room temperature, a solution of isopropyl bromide (814 mg, 6.64 mmol) in 10 ml dry DMF was added and the mixture heated to 80° C. After stirring for additional 48 h, the mixture was cooled to room temperature and diluted with 150 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 4/1, Rf=0.21) gave 6-bromo-1-isopropyl-3,4-dihydro-1H-quinolin-2-one (347 mg, 1.29 mmol, 33%) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541404B2
Source datasetuspto-grants-2013_09
ORD IDord-5ceeb796fc7647d8bdb01bfa4f4dd658
Source noteuspto-grants-2013_09