HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 1,3-Dioxane-4-acetamide, 6-(cyanomethyl)-2,2-dimethyl-N,N-diphenyl-, (4R-cis)-(9CI)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | 6-cyano-3,5-dihydroxy-N,N-diphenylhexanamide | HCID 22415340 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3-Dioxane-4-acetamide, 6-(cyanomethyl)-2,2-dimethyl-N,N-diphenyl-, (4R-cis)-(9CI) | HCID 10883013 | — |
Reaction Steps
Crude R-(R*,R*)!-6-cyano-3,5-dihydroxy-N,N-diphenylhexanamide, approximately 0.18 mol, is dissolved in 2,2-dimethoxypropane (160 mL, 1.5 mol) and acetone (300 mL). Methanesulfonic acid (0.5 mL) is added, and the solution is stirred for 2 hours at room temperature. The reaction is quenched by the addition of aqueous sodium bicarbonate (800 mL) and ethyl acetate (500 mL). The ethyl acetate solution is concentrated by vacuum distillation to give 62.5 g of (4R-cis)-6-(cyanomethyl)-2,2-dimethyl-N,N-diphenyl-1,3-dioxane-4-acetamide as an off-white crystalline solid (mp 98°-100° C., uncorrected).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05510488 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-727ed4f4f0bc4ec596df7858fd15a342 |
| Source note | uspto-grants-1996_04 |