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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158387Generated: November 1, 2026

Hydrochloric Acid → HCID 59512399, compound

https://huagongshe.com/reaction/1158387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Methoxy-propyl)-3-methyl-1H-indole-6-carboxylic acid methyl esterHCID 67541972—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 59512399HCID 59512399—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(3-methoxy-propyl)-3-methyl-1H-indole-6-carboxylic acid methyl ester (1.56 g, 6.3 mmol) in MeOH (20 mL) and H2O (1 mL) is added NaOH (756 mg, 18.9 mmol) and the mixture is stirred at 50° C. overnight. Then neutralized by the addition of water and HCl 1.0 M (3 eq, 18.9 mmol). CH2Cl2 is added, the layers are separated, and the aqueous one is extracted twice with CH2Cl2. The combined organic layers are dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material is obtained in a pure form and is used in the next step without purification. MS (LC-MS): 248.0 [M+H]+; tR (HPLC, Macherey-Nagel Nucleosil C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/3 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 4.93 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-c073ffabeca843be82aa6cdd79dcdd84
Source noteuspto-grants-2010_10