HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-heptyl-N-ethyl(6-hydroxy)hexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-heptyl-N-ethyladipamic acid, methyl ester | HCID 86748668 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | N-heptyl-N-ethyl(6-hydroxy)hexanamide | HCID 22407916 | 35.8% |
Reaction Steps
A mixture of a solution of 3.1 gms of the N-heptyl-N-ethyladipamic acid, methyl ester in 40 ml of tert-butanol and 800 mg of sodium borohydride is heated to reflux, following which 7.8 ml of methanol is added dropwise. The reaction mixture is stirred at reflux for 18 hours and then partitioned between water and CH2Cl2. After separation, the organic layer is dried over MgSO4, filtered, and concentrated under vacuum. The residue obtained is flash chromatographed on normal phase silica gel with a 4/1 ratio of hexane and ethyl acetate to yield 1.0 gms of N-heptyl-N-ethyl(6-hydroxy)hexanamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05412137 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-6a455df6206d4f0fa050d33537601b1c |
| Source note | uspto-grants-1995_05 |