HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyl-D-glucamine → N-methyl-N-[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]docosanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyl-D-glucamine | HCID 8567 | — |
| Reactant | Docosanoyl chloride | HCID 4104741 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-methyl-N-[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]docosanamide | HCID 15218940 | 29.4% |
Reaction Steps
N-Methyl glucamine (1.95 g, 10.0 mmol) was dissolved in 10 mL of 1.00 N sodium hydroxide solution and 10 mL of tetrahydrofuran. Docosanoyl chloride (3.58 g, 10.0 mmol) was then added to the rapidly stirred solution followed by another 20 mL portion of tetrahydrofuran. After stirring for 60 min, the thick reaction mixture was placed on a rotary evaporator and tetrahydrofuran was removed under reduced pressure. The resulting thick slurry was filtered, washed with water and dried with suction to give a waxy white solid. Chromatography (SiO2, 15%-30% MeOH/CHCl3) yielded 1.52 g of the following compound as a waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557893B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-11fa651d44cf4445ad9527da40e0d4c6 |
| Source note | uspto-grants-2013_10 |