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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant6-Methoxy-1H-indole-3-carboxylic acidHCID 17750956—
SolventDimethylformamideHCID 6228—
Product1-tert-Butoxycarbonylmethyl-6-methoxy-1H-indole-3-carboxylic acidHCID 68283464—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-3d6e7ffe48cb4f5a9604760818abbb59
Source noteuspto-grants-2015_07