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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 58338541 | HCID 58338541 | — |
| Reactant | HCID 131730192 | HCID 131730192 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-(4-(6-Methoxy-2-(5-(methylsulfinyl)thiophen-2-yl)naphthalen-1-yloxy)phenoxy)ethyl)piperidine | HCID 58338560 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476300B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ff85a319f1df4f0c86f480029cdf1ec1 |
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| Source note | uspto-grants-2013_07 |
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