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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769350Generated: November 2, 2026

Ethyl bromoacetate → HCID 18947548, compound

https://huagongshe.com/reaction/1769350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18947557HCID 18947557—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18947548HCID 18947548—

Reaction Steps

To 91 mg of 2-[N-(p-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-ylmethoxy)indol-2-yl]ethanol from Step B in 2 mL THF at 0° C. under an argon atmosphere was added 40 mg of 80% sodium hydride over 30 min. Ethyl bromoacetate (0.3 ml) was added to the solution and the reaction stirred at RT overnight. The reaction was poured onto 10 mL of NH4OAc (25% solution), extracted with 3×10 mL of EtOAc, washed with 20 mL of H2O and dried over MgSO4. Removal of the solvent followed by column chromatography on silica gel afforded the ethyl ester of title compound. Hydrolysis of this ester under the conditions described in Step B of Example 1 provided the title compound, m.p. 185° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380850
Source datasetuspto-grants-1995_01
ORD IDord-4d74442aae92490186fa8115d94455e4
Source noteuspto-grants-1995_01