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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091162Generated: November 2, 2026

Ammonium Chloride → HCID 66777421, compound

https://huagongshe.com/reaction/2091162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Chloro-3-methyl-1-benzofuran-2-carbaldehydeHCID 4736982—
ReactantHCID 178418816HCID 178418816—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66777421HCID 6677742150%

Reaction Steps

To a solution (20 mL) of 5-chloro-3-methyl-1-benzofuran-2-carbaldehyde (1.00 g) synthesized in Example A88(2) in tetrahydrofuran was added a 1.0M solution (10.3 mL) of isobutylmagnesium bromide in tetrahydrofuran at 0° C., and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20% ethyl acetate/hexane) to give the title object compound (650 mg, 50%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-0593f3c38ebd4f2990b6ea2a2c5d9488
Source noteuspto-grants-2013_05