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HRID 1154783作成日:2026年10月26日

Ammonia → Oxendolone

https://huagongshe.com/reaction/1154783

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物TetrahydrofuranHCID 8028—
反応物LithiumHCID 3028194—
反応物16beta-Ethyl-3-methoxy-1,3,5(10)-estratrien-17beta-olHCID 12831647—
溶媒tert-ButanolHCID 6386—
生成物OxendoloneHCID 443947—

反応条件

温度50 °C

反応手順

A solution of 2.0 g. of 16β-ethyl-3-methoxy-1,3,5(10)-estratrien-17β-ol in 40 ml. of tetrahydrofuran and 4 ml. of tert.-butanol is added dropwise at -40° C. to 80 ml. of ammonia. After the incremental introduction of 1.2 g. of lithium, the mixture is stirred for 2 hours at -40° C.; then the ammonia is allowed to evaporate, the residue is poured into about 200 ml. of water, and the mixture is extracted with ethyl acetate. The crude product is taken up in 40 ml. of methanol and 4 ml. of 4 N hydrochloric acid and agitated for 15 minutes at 50° C. Thereafter, the mixture is poured into water and extracted with methylene chloride. After recrystallizing the crude product from ethyl acetate/ether, 1.7 g. of 16β-ethyl-17β-hydroxy-4-estren-3-one is produced, m.p. 150°-152° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04298538
出典データセットuspto-grants-1981_11
ORD IDord-a7e1eac35c894d3aabd07696fa222da2
出典メモuspto-grants-1981_11