تفاعل #160830
ord-b2e4355bacd546f2952490ef96acf714
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىA 5 L 4-neck round bottom flask (rbf) fitted with an overhead stirrer
- 2workup.ADDITIONa thermocouple was charged with
- 3workup.ADDITIONadded all at once)
- 4أخرىrose to 22° C
- 5ترشيحfiltered
- 6workup.WAITThe crude material was left on the frit
- 7workup.WAITto drain for one hour
- 8workup.STIRRINGvigorously stirred for five minutes (no more than 10 min)
- 9ترشيحfiltered again
- 10غسيلwashing 2× with ice cold water
- 11workup.WAITleft
- 12أخرىto dry overnight on the fritted filter
- 13أخرىThe partially dried material was dried for 12 h in a vacuum oven (50° C., 0.1 torr)
- 14أخرىwell crushed with a mortar & pestal
- 15أخرىAn additional 16 h of drying in the vacuum oven
الإجراء التجريبي
A 5 L 4-neck round bottom flask (rbf) fitted with an overhead stirrer & a thermocouple was charged with; (1) a solution of NaOH (60.85 g, 1.52 mol, 2.4 eq) in 180 mL water, (2) a solution of hydroxylamine-HCl (110.12 g, 1.58 mol, 2.5 eq) in 180 mL water and (3) 180 mL dioxane. The mixture was cooled in an ice/acetone bath to 0° C. 150 g of ice was added, followed by a precooled (to about 10° C.) solution of diphenylphosphinic chloride (150.0 g, 0.634 mol, 1 eq) in 180 mL dioxane (added all at once). The reaction became very thick with a white precipitate, requiring vigorous stirring. The internal temperature rose to 22° C. After 5 additional minutes stirring (10 minutes maximum), the reaction mixture was diluted with 2.5 L of ice cold water and filtered thru a large fritted funnel (15 cm diameter). The crude material was left on the frit to drain for one hour, then transferred back into the 5 L rbf. The solid was suspended in 500 mL ice cold 0.25N NaOH solution and vigorously stirred for five minutes (no more than 10 min), then filtered again, washing 2× with ice cold water and left to dry overnight on the fritted filter. The partially dried material was dried for 12 h in a vacuum oven (50° C., 0.1 torr) and then well crushed with a mortar & pestal. An additional 16 h of drying in the vacuum oven afforded 122 g (82%) the above compound as a white powder.