HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054577Generated: November 2, 2026
2-Methyl-2-butene → 6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1054577
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Phosphate, Monobasic, Monohydrate | HCID 516949 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | 6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carbaldehyde | HCID 86698580 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 6-fluoro-5-[4-(hydroxymethyl)phenyl]-1H-indole-3-carboxylic acid | HCID 86698581 | 29.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394285B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-33b50446266147c68623b7401ae320e4 |
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| Source note | uspto-grants-2016_07 |
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