تفاعل #95510
ord-d4221ef4e3074261a4eed3b243a596f9
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.ADDITIONA mixture of 1.55 ml
- 2أخرىthe organic layer is separated
- 3غسيلwashed with water
- 4أخرىdried
- 5تركيزrefrigerated and then concentrated to an oil
- 6أخرىgiving 8.3 g
- 7workup.DISSOLUTIONThis oil is dissolved in 30 ml
- 8workup.WAITto stand for 3 hours
- 9درجة الحرارةheated at 45°-50° C. for 3 hours, refrigerated overnight
- 10تركيزconcentrated to about 1/3 its original volume
- 11workup.ADDITIONAn equal volume of ether is added
- 12أخرىproducing a gum
- 13أخرىThe solvent is removed
- 14workup.ADDITIONof ammonium hydroxide are added
- 15أخرىThe solid is collected
- 16غسيلwashed with water
- 17أخرىdried
- 18workup.DISSOLUTIONdissolved in 25 ml
- 19ترشيحfiltered and to the filtrate
- 20workup.ADDITIONare added alcoholic hydrogen chloride and ether
- 21ترشيحAfter refrigeration, the solid is filtered
- 22غسيلwashed with ether
- 23ترشيحof ethanol and filtered
- 24workup.ADDITIONThe filtrate is treated with alcoholic hydrogen chloride
- 25درجة الحرارةcooled
- 26أخرىgiving 0.41 g
الإجراء التجريبي
A mixture of 1.55 ml. of methanesulfonyl chloride and 40 ml. of toluene is added over a period of one hour to a stirred mixture of 5.8 g. of 4'-chloro-3,4-(methylenedioxy)benzoin, 5.6 ml. of triethylamine and 20 ml. of toluene. The mixture is allowed to stand 4 hours, 50 ml. of water and more toluene are added, the organic layer is separated, washed with water, dried, refrigerated and then concentrated to an oil, giving 8.3 g. of the methanesulfonate ester. This oil is dissolved in 30 ml. of acetone and added to a stirred mixture of 1.95 g. of hexahydro-2H-1,3-diazepin-2-thione in 150 ml. of acetone. The mixture is allowed to stand for 3 hours, heated at 45°-50° C. for 3 hours, refrigerated overnight and concentrated to about 1/3 its original volume. An equal volume of ether is added producing a gum. The solvent is removed, 100 ml. of water and 2 ml. of ammonium hydroxide are added. The solid is collected, washed with water, dried and dissolved in 25 ml. of ethanol. This solution is refrigerated, then filtered and to the filtrate are added alcoholic hydrogen chloride and ether. After refrigeration, the solid is filtered, washed with ether, boiled with 25 ml. of ethanol and filtered. The filtrate is treated with alcoholic hydrogen chloride and cooled, giving 0.41 g. of the desired product, m.p. 184°-186° C.