HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2463Generated: October 26, 2026
Sodium Bicarbonate → N-(2-hydroxyethyl)-3-methoxy-N-(2-methoxyphenyl)benzamide
https://huagongshe.com/reaction/2463
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 3-Methoxy-N-(2-methoxyphenyl)-N-(2-tetrahydropyranyloxyethyl)benzamide | HCID 53926084 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-hydroxyethyl)-3-methoxy-N-(2-methoxyphenyl)benzamide | HCID 19689855 | 86.8% |
Reaction Steps
3-Methoxy-N-(2-methoxyphenyl)-N-(2-tetrahydropyranyloxyethyl)benzamide (501 mg, 1.30 mmol) was dissolved in methanol (4 ml) to which was subsequently added a catalytically effective amount of p-toluenesulfonic acid monohydrate and stirred for 3 hours at room temperature. The reaction solution was mixed with saturated sodium bicarbonate aqueous solution (10 ml) and extracted with ether, and then washed with water and saturated brine. The resulting organic layer was dried on anhydrous magnesium sulfate, the solvent was removed by evaporation and then the resulting colorless oily residue was purified by subjecting it to a silica gel column chromatography (ether:hexane=3:1) to obtain 340 mg (86.8%) of the title compound in the form of light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728835 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-cbf5b75d0c184a8f8de856d128b7a42f |
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| Source note | uspto-grants-1998_03 |
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