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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338301Generated: October 26, 2026

2-Methyl-2-butene → 6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/338301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Reactant6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carbaldehydeHCID 86698646—
SolventWaterHCID 962—
SolventAcetonitrile tert-butanolHCID 22050040—
Product6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carboxylic acidHCID 8669864738%

Reaction Steps

To a solution of 6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carbaldehyde (100 mg, 0.35 mmol) in ACN/t-butanol=1/1(4 mL) was added 2-methyl-2-butene (1 mL) at 0° C. and stirred 10 min. Then an aqueous solution of sodium chlorite (315 mg, 3.5 mmol) and sodium dihydrogen phosphate (480 mg, 3.5 mmol) in water (1 mL) was added to the system dropwise. The reaction was stirred at room temperature for 10 h. The reaction was quenched with sodium sulfite. The mixture was partitioned between DCM and water. The combined organics were dried and concentrated to give a residue, which was purified by reverse phase HPLC to give the title compound (40 mg, 38%) as a white solid. MS (AP−) 300.1 (M−1)−. 1H NMR (400 MHz, CD3OD) δ 8.01 (s, 1H), 8.00 (s, 1H), 7.58 (s, 1H), 7.33 (t, 1H), 7.01-6.97 (m, 2H), 6.93 (dd, 1H), 3.84 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-c193719438a14e1a9c85280d3ff587fe
Source noteuspto-grants-2014_11