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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374791Generated: October 30, 2026

Ethyl bromoacetate → HCID 123817435, compound

https://huagongshe.com/reaction/1374791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22034371HCID 22034371—
ProductHCID 123817435HCID 123817435—

Reaction Steps

To a stirred solution of sodium hydride (45 mg of 60% dispersion in mineral oil) in dry tetrahydrofuran (10 ml) was added 3-[(4-chlorophenyl)thio]-2-methyl-6-(methylsulfonyl)-1H-indole (160 mg) (the product of Example 20 step i). After 30 minutes the reaction was treated with ethyl bromoacetate (78 μl) and stirring continued for 1 hour. Reaction was quenched with ethanol, the solvent was removed in vacuo, the residue redissolved in ethyl acetate, washed with water, dried (MgSO4), and evaporated in vacuo and the residue purified by flash column chromatography eluting with 30% ethyl acetate and iso-hexane mixture. The sub-title compound was obtained as a white solid (180 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166607B2
Source datasetuspto-grants-2007_01
ORD IDord-16c3b861494c4e8c917cee12648ff35a
Source noteuspto-grants-2007_01