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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091020Generated: November 1, 2026

Nitromethane → HCID 66777743, compound

https://huagongshe.com/reaction/2091020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantIsovaleryl chlorideHCID 66054—
Reactant3-Methylbenzo[b]thiopheneHCID 73817—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
ProductHCID 66777743HCID 6677774399%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 3-methyl-1-benzothiophene (5.00 g), isovaleryl chloride (4.52 mL) and nitromethane (50 mL) was added aluminum (III) chloride (8.98 g) at 0° C., and the mixture was stirred at 0° C. for 30 min then at room temperature for 4 hr. The reaction mixture was poured into ice-cooled water, and the mixture was extracted with ethyl acetate. The extract was washed with 1N hydrochloric acid and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:19, volume ratio) to give the title object compound (7.72 g, 99%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-dbf0a1b6d781423bbeccf57b9040dcca
Source noteuspto-grants-2013_05