HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393667Generated: November 2, 2026
Hydrochloric Acid → 1-[(Acetyloxy)methyl]-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1393667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethyl acetate | HCID 68536 | — |
| Reactant | Indole-3-Carboxylic Acid | HCID 69867 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(Acetyloxy)methyl]-1H-indole-3-carboxylic acid | HCID 23091967 | 61% |
Reaction Steps
1H-Indole-3-carboxylic acid (400 mg) was dissolved in N,N-dimethylformamide (6 ml) and cooled to 0° C. Sodium hydride (500 mg) was added to the solution in two divided portions, and the mixture was stirred as such for 30 minutes. Bromomethyl acetate (0.32 ml) was added slowly dropwise thereto, and the mixture was stirred for 15 minutes at 0° C., warmed to room temperature and stirred for 45 minutes. The mixture was cooled to 0° C., and water was added to the mixture which was then acidified by 2 N hydrochloric acid and extracted with ethyl acetate. The extract was dried over sodium sulfate anhydrous and concentrated under reduced pressure. The residue was purified by column chromatography (eluting solvent; dichloromethane:methanol 50:1) to give the title compound (354 mg, Y.:61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07345180B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-d184009954a14e19a2dd781002a6dc3c |
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| Source note | uspto-grants-2008_03 |
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