Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Methoxy-6-(3-methoxyphenyl)-1-naphthoic acid | HCID 59443481 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59443439 | HCID 59443439 | — |
Reaction Steps
2-Methoxy-6-(3-methoxyphenyl)-1-naphthoic acid (200 mg, 0.65 mmol, 1 eq) is boiled under reflux with 5 ml of thionyl chloride under a nitrogen atmosphere for 30 min according to method E. The residue is dissolved in dry THF and added to 1 ml of morpholine cooled at 0° C. The reaction mixture is boiled under reflux over night. After the solvent has been removed on a rotary evaporator, purification is effected by column chromatography with dichloromethane/methanol 95/5 as the eluent. Characterization of the compound was not effected. The raw product was directly employed for ether cleavage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546392B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-5b5fbccba8be49ee8b4502e0177f6fb4 |
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| Source note | uspto-grants-2013_10 |
|---|