Sodium Hydroxide → HCID 58931881, compound
Reaction equation
Cl.[CH:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([CH2:5]3)[CH:3]1[NH2:12])[CH2:9]2.[OH-].[Na+].Cl[CH2:16][CH:17]([OH:23])[CH2:18][S:19]([OH:22])(=[O:21])=[O:20].[Na]>O1CCOCC1.O>[CH:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([CH2:5]3)[CH:3]1[NH:12][CH2:16][CH:17]([OH:23])[CH2:18][S:19]([OH:22])(=[O:21])=[O:20])[CH2:9]2Participants
Conditions
- Temperature
- 80 °C
Procedure
To an 80° C. solution of 2-adamantanamine hydrochloride (2.50 g, 13.3 mmol) and sodium hydroxide (586 mg, 14.6 mmol) in 1,4-dioxane (7 mL) and water (7 mL) was added via syringe pump (1 hour addition) a solution of 3-chloro-2-hydroxy-propane sulfonic acid, sodium salt (1.76 g, 8.9 mmol) in 1,4-dioxane (1 mL) and water (9 mL). The solution was stirred at 80° C. for an additional 4 hours. The reaction was cooled to room temperature. The solvent was evaporated under reduced pressure. The solid was suspended in EtOH (25 mL). The mixture was heated to reflux for 1 minute. The solid was removed by filtration. The pure product crystallized in the filtrate. The product was filtered, washed with EtOH (1×10 mL) and dried in vacuo. Yield: 30%. 1H NMR (D2O, 500 MHz) δ ppm 4.30 (m, 1H), 3.35 (m, 2H), 3.03 (m, 3H), 2.07 (m, 2H), 1.84 (m, 2H), 1.75 (m, 4H), 1.65 (d, 6H). 13C (D2O, 125 MHz) δ ppm 63.31, 55.03, 49.51, 36.51, 36.33, 36.26, 29.78, 29.23, 28.81, 26.63, 26.38. ES-MS 289 (M+1).
Workup
- temperatureThe reaction was cooled to room temperature
- customThe solvent was evaporated under reduced pressure
- temperatureThe mixture was heated
- temperatureto reflux for 1 minute
- customThe solid was removed by filtration
- customThe pure product crystallized in the filtrate
- filtrationThe product was filtered
- washwashed with EtOH (1×10 mL)
- customdried in vacuo
Sources & evidence
- ORD record
- ord-bf97edad53474f68bc7e946820cb9753
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642801B2
Reaction notes
Loading…