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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | 6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carbaldehyde | HCID 86698646 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile tert-butanol | HCID 22050040 | — |
| Product | 6-chloro-5-(3-methoxyphenyl)-1H-indole-3-carboxylic acid | HCID 86698647 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889730B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-c193719438a14e1a9c85280d3ff587fe |
|---|
| Source note | uspto-grants-2014_11 |
|---|