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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925261Generated: October 28, 2026

Hydrochloric Acid → 6-Bromonaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/1925261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant6-bromo-N-methoxy-N-methyl-2-NaphthalenecarboxamideHCID 59813225—
SolventTetrahydrofuranHCID 8028—
Product6-Bromonaphthalene-2-carbaldehydeHCID 13477029—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 6-bromo-naphthalene-2-carboxylic acid methoxy-methyl-amide (Step c, 6.3 g, 21.4 mmol) in THF (200 mL) at −78° C., DIBAL (1M in THF, 25.7 mL, 25.7 mmol) was added. The mixture was stirred at −78° C. for 10 min, warmed to RT and stirred for 2 h. The reaction was poured into 1N HCl and extracted with EtOAc 3×. The combined organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude was purified by silica gel column chromatography with (5-20% EtOAc/hexane) to give the titled compound as a white solid. MS (ESI, pos. ion) m/z: 236.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-fb008dc4ebca4f0db4539d454e8cb443
Source noteuspto-grants-2012_05