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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338234Generated: October 31, 2026

2-Methyl-2-butene → 6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/338234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium Phosphate, Monobasic, MonohydrateHCID 516949—
ReactantSodium ChloriteHCID 23668197—
Reactant6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carbaldehydeHCID 86698580—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solventtert-ButanolHCID 6386—
Product6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carboxylic acidHCID 8669858129.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carbaldehyde (65 mg, 0.24 mmol) in acetonitrile (3 mL) and tert-butanol (3 mL) was treated with 2-methyl-2-butene (2 mL, 18.4 mmol) and cooled to 0° C. A solution of sodium chlorite (410 mg, 4.9 mmol) and sodium dihydrogen phosphate monohydrate (684 mg, 4.96 mmol) in water (3 mL) was added dropwise via an addition funnel. The reaction mixture was warmed to room temperature and stirred for 65 hours. The reaction was partially evaporated in vacuo, and partitioned between water and ethyl acetate. The organic phase was concentrated in vacuo. The crude material was purified using reverse-phase chromatography to give the title compound (20.4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-f87324e8a05b4325b2b6cb578d757ebb
Source noteuspto-grants-2014_11