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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(3,4-dihydro-2H-1-benzopyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 43811034 | — |
| Reactant | methyl 2-(2-bromo-1-methyl-1H-indol-3-yl)pentanoate | HCID 70819053 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-1-methyl-1H-indol-3-yl]pentanoate | HCID 70855400 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238026B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-8fb792da203b4b21b3270f8714fef202 |
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| Source note | uspto-grants-2016_01 |
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