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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338316Generated: October 29, 2026

2-Methyl-2-butene → HCID 86698663, compound

https://huagongshe.com/reaction/338316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium Phosphate, Monobasic, MonohydrateHCID 516949—
ReactantSodium ChloriteHCID 23668197—
ReactantHCID 86698664HCID 86698664—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86698663HCID 86698663—

Reaction Steps

A solution of 5-[4-(1-{[tert-butyl(dimethyl)silyl]oxy}-2-methylpropan-2-yl)phenyl]-6-chloro-1H-indole-3-carbaldehyde (130 mg, 0.294 mmol) in tetrahydrofuran (2.5 mL) and tert-butanol (2.5 mL) was treated with 2-methyl-2-butene (2.19 mL, 20.6 mmol) followed by a solution of sodium chlorite (496 mg, 5.9 mmol) and sodium phosphate monobasic hydrate (811 mg, 5.9 mmol) in water (2.5 mL) via glass pipet at room temperature. The reaction mixture was stirred vigorously at room temperature for 15 hours, and was poured into saturated aqueous ammonium chloride solution (35 mL). The product was extracted with ethyl acetate (3×25 mL), and the combined organic layers were dried over sodium sulfate, filtered and evaporated to give the title compound as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-b414a741e61f4ef5a38066bc8e6a2da1
Source noteuspto-grants-2014_11