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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240793Generated: October 31, 2026

Isopropyl iodide → 3-Isopropyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid

https://huagongshe.com/reaction/2240793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantHCID 57508882HCID 57508882—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178418306HCID 178418306—
Product3-Isopropyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acidHCID 5750888620.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled solution (−78° C.) of 5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (2.00 g, 9.51 mmol) in THF (35 mL), tert.-butyllithium (16 mL, 1.5 M solution in pentane) is added. The mixture is stirred at −78° C. for 10 min before isopropyliodide (7.60 g, 48.7 mmol) is added. The reaction mixture is stirred at −78° C. for 3 h, then at rt for 3 d. The reaction mixture is diluted with water and extracted twice with EA. The combined organic extracts are dried over Na2SO4 and evaporated. The crude product is purified by CC on silica gel eluting with DCM/TBME 20:1 followed by prep. HPLC to give 3-isopropyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (500 mg) as a white solid; LC-MS: tR=1.04 min, [M+1+CH3CN]=294.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723378B2
Source datasetuspto-grants-2010_05
ORD IDord-4dbacdc7dee54f8ebbe44bad12896759
Source noteuspto-grants-2010_05