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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375264Generated: October 25, 2026

Carbon Dioxide → 1(5-Methyl-thien-2-yl)3,4-dihydro-4,4-diethyl-7-naphthaldehyde

https://huagongshe.com/reaction/1375264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDimethylformamideHCID 6228—
ReactantPentaneHCID 8003—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthaleneHCID 18620062—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product1(5-Methyl-thien-2-yl)3,4-dihydro-4,4-diethyl-7-naphthaldehydeHCID 21079515—

Reaction Steps

To a cold (−78° C.) solution of 1-(5-methyl-thien-2-yl)-3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene (Compound F, 1.35 g, 4.1 mmol), in THF (20 mL) was added t-BuLi in pentane (1.7M solution, 3.5 mL, 5.95 mmol). The reaction was stirred for 15 minutes. and DMF (600 mg, 5.8 mmol) was added and dry-ice cooling was replaced with ice-water bath. The mixture was stirred at ambient temperature for 4 hours. The reaction mixture was diluted with ether (70 mL) and washed with water (5 mL), brine (5 mL) and dried with MgSO4. Solvent was removed by distillation. The product was purified by silicagel chromatography to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166726B2
Source datasetuspto-grants-2007_01
ORD IDord-0dfef76ef84349f897b21b46838ad55b
Source noteuspto-grants-2007_01