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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297988Generated: October 31, 2026

Acetic Acid → 1-(2-Trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/2297988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-indole-5-carboxylateHCID 2737635—
Reactant2-(Trimethylsilyl)ethane-1-sulfonyl chlorideHCID 9837086—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl esterHCID 5438486277.6%

Reaction Steps

To a solution of 1H-indole-5-carboxylic acid methyl ester (3.6 g, 20.6 mmol) in tetrahydrofuran (180 mL) at 0° C., was added sodium hydride (0.65 g, 21.9 mmol). After 10 min., 2-trimethylsilanylethanesulfonyl chloride (4.4 g, 21.9 mmol) was added and the reaction mixture was allowed to warm to room temperature. After 3 h, acetic acid (1.6 mL, 26.8 mmol) was added and the reaction mixture was concentrated. The crude product was chromatographed (Biotage 40M column, 2.5% ethyl acetate-hexanes) to afford 1-(2-trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl ester (5.43 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492394B1
Source datasetuspto-grants-2002_12
ORD IDord-d7e567e00ed04a6bbe77a4a32ab8ccc0
Source noteuspto-grants-2002_12