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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836878Generated: October 26, 2026

2-Nitropropane → 3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/1836878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitropropaneHCID 398—
ReactantSodiumHCID 5360545—
Reactant6-Bromo-7-(bromomethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 23498953—
SolventEthanolHCID 702—
Product3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehydeHCID 1778988761%

Reaction Steps

0.981 g (42.7 mmol) of sodium was dissolved in 50 mL of ethanol. To this solution was added 4.94 g (55.5 mmol) of 2-nitropropane followed by 17.3 g (42.7 mmol) of crude 2-bromo-3-bromomethyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene in 75 mL ethanol. After 8 hours, this mixture was concentrated in vacuo and then partitioned between ethyl acetate and water. The organic layer was sequentially washed with 1M aqueous sodium hydroxide, water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The product was purified by flash chromatography on silica gel with gradient elution (1-2% ethyl acetate/hexane) to afford 7.63 g (61%) of 3-bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthaldehyde (m.p.=113.9-114.3° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777418B2
Source datasetuspto-grants-2004_08
ORD IDord-2af467902f154c71b5c884f5c0714369
Source noteuspto-grants-2004_08