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HRID 268037作成日:2026年10月27日

Ammonia → 6,11-Dihydro-(alpha-methyl)-11-oxo-dibenzo[b,e]thiepine-2-acetic acid ethyl ester

https://huagongshe.com/reaction/268037

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Methyl iodideHCID 6328—
反応物SodiumHCID 5360545—
反応物6,11-Dihydro-11-oxo-dibenzo[b,e]thiepine-2-acetic acid ethyl esterHCID 44407646—
触媒Ferric nitrateHCID 25251—
溶媒Diethyl EtherHCID 3283—
生成物6,11-Dihydro-(alpha-methyl)-11-oxo-dibenzo[b,e]thiepine-2-acetic acid ethyl esterHCID 54497536—

反応手順

2.4 G of finely cut sodium are added portionwise to 300 cc of ammonia condensed at -40°, with the addition of 200 mg of iron (III) nitrate. Stirring is effected for 30 minutes at the same temperature and 300 cc of ether are subsequently allowed to flow slowly into the reaction mixture. 31.2 g of 6,11-dihydro-11-oxo-dibenzo[b,e]thiepine-2-acetic acid ethyl ester are subsequently added portionwise. After 15 minutes, the salt formation is complete. 17.0 G of methyl iodide in 100 cc of ether are added dropwise at -40°. After a further 15 minutes, the reaction is complete. The ammonia is removed by evaporation and successively replaced by 300 cc of ether. The organic phase is finally shaken with 50 g of ammonium chloride dissolved in water and is washed with water until neutral. The solution which has been purified with charcoal and dried over sodium sulphate, is concentrated at reduced pressure and pentane is added thereto, whereby 6,11-dihydro-(α-methyl)- 11-oxo-dibenzo[b,e]thiepine-2-acetic acid ethyl ester crystallies. M.P. 91°-93°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03946036
出典データセットuspto-grants-1976_03
ORD IDord-afc5d12bb7e04b91825fa7b6372c6f76
出典メモuspto-grants-1976_03