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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445207Generated: October 29, 2026

Methanol → 1-(2-(4-(6-Methoxy-2-(5-(methylsulfinyl)thiophen-2-yl)naphthalen-1-yloxy)phenoxy)ethyl)piperidine

https://huagongshe.com/reaction/445207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 58338541HCID 58338541—
ReactantHCID 131730192HCID 131730192—
SolventWaterHCID 962—
Product1-(2-(4-(6-Methoxy-2-(5-(methylsulfinyl)thiophen-2-yl)naphthalen-1-yloxy)phenoxy)ethyl)piperidineHCID 58338560—

Reaction Conditions

Temperature0 °C

Reaction Steps

Add 1-(2-(4-(6-methoxy-2-(5-(methylthio)thiophen-2-yl)naphthalen-1-yloxy)phenoxy)ethyl)piperidine (84 mg, 0.17 mmol), tetrahydrofuran (3.3 mL) and methanol (3.3 mL) to a round bottom flask under nitrogen. Cool the resulting solution to 0° C. and add solution of potassium peroxymonosulfate sulfate (102 mg; 0.17 mmol) in water (1.7 mL). Stir the resulting mixture at 0° C. for 30 min. Load the mixture onto an SCX acidic ion exchange column. Flush the column with 1:1 methanol/dichloromethane and elute with 1:1 2M ammonia in methanol/dichloromethane. Concentrate the ammonia containing eluent in vacuo to give the title compound (87 mg, 0.17 mmol): mass spectrum (m/z): 522 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476300B2
Source datasetuspto-grants-2013_07
ORD IDord-ff85a319f1df4f0c86f480029cdf1ec1
Source noteuspto-grants-2013_07