HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527207Generated: November 4, 2026
Hydrochloric Acid → 1-tert-Butoxycarbonylmethyl-6-methoxy-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1527207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 6-Methoxy-1H-indole-3-carboxylic acid | HCID 17750956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-tert-Butoxycarbonylmethyl-6-methoxy-1H-indole-3-carboxylic acid | HCID 68283464 | — |
Reaction Steps
To an ice-cooled suspension of 6-methoxy-1H-indole-3-carboxylic acid (1 g, 5.23 mmol) in DMF (35 mL) was added NaH (60% suspension in oil; 0.523 g, 13.1 mmol) in one portion, and the mixture was stirred at 0° C. for 30 min. Tert-butyl-2-bromoacetate (0.85 mL, 5.75 mmol) was then added dropwise, and stirring was continues at RT overnight. The reaction mixture was neutralized by addition of saturated NH4Cl, and the solution was then adjusted to pH=2-3 by addition of 0.1N HCl. The aqueous layer was repeatedly extracted with CH2Cl2, the combined organics were washed with brine, dried (phase separator) and concentrated in vacuo. The residue was dissolved in a small volume of methanol, followed by addition of water until a solid precipitated. The precipitate was filtered off, washed with water and dried in vacuo to afford the title compound as a white solid. MS (LC/MS): 306 [M+H]+, 328 [M+Na]+; tR (HPLC conditions c): 4.67 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085555B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-3d6e7ffe48cb4f5a9604760818abbb59 |
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| Source note | uspto-grants-2015_07 |
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