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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591000Generated: October 30, 2026

Water → methyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-1-methyl-1H-indol-3-yl]pentanoate

https://huagongshe.com/reaction/591000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-(3,4-dihydro-2H-1-benzopyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 43811034—
Reactantmethyl 2-(2-bromo-1-methyl-1H-indol-3-yl)pentanoateHCID 70819053—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethylformamideHCID 6228—
Productmethyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-1-methyl-1H-indol-3-yl]pentanoateHCID 7085540086%

Reaction Conditions

Temperature110 °C

Reaction Steps

Under a nitrogen atmosphere, sodium carbonate (370 mg, 3.5 mmol), water (20 mL), palladium tetrakis(triphenylphosphine) (620 mg, 0.54 mmol) and 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chroman (904 mg, 3.48 mmol) were added to a solution of methyl 2-(2-bromo-1-methyl-1H-indol-3-yl)pentanoate (1.13 g, 3.4 mmol) in N,N-dimethylformamide (80 mL). The mixture was heated at 110° C. for 2 hours, concentrated in vacuo and water (40 mL) was added. The aqueous layer was extracted with ethyl acetate (2×20 mL). The organic layer was washed with brine (20 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 95/5) to afford the desired product (12d) as a white solid (1.1 g, 2.91 mmol, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-8fb792da203b4b21b3270f8714fef202
Source noteuspto-grants-2016_01