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HRID 371964作成日:2026年10月25日

Ammonia → Cyclohexanone, trimethyl-

https://huagongshe.com/reaction/371964

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物WaterHCID 962—
反応物1,4-Dichloro-2-buteneHCID 15122—
反応物2,2,6-TrimethylcyclohexanoneHCID 17000—
溶媒TetrahydrofuranHCID 8028—
生成物Cyclohexanone, trimethyl-HCID 301657019.6%

反応手順

28 g of 2,2,6-trimethyl-cyclohexanone are added dropwise to a suspension of Na vinylacetylide (prepared from 25 g of 1,4-dichlorobut-2-ene and 15 g of Na in liquid ammonia) in 200 ml of THF, whilst cooling, and the reaction mixture is stirred overnight at room temperature. 50 ml of water are then added, the aqueous phase is extracted with ether and the resulting organic phase is dried and concentrated. Subsequent fractional distillation gives 5.5 g of unconverted trimethylcyclohexanone and 20.7 g (corresponding to 68% of theory, based on ketone converted) of 2,2,6-trimethyl-1-(but-1'-yn-3'-en-1'-yl)-cyclohexanol of boiling point 62°-63° C/0.3 mm Hg and refractive index nD25 = 1.4982. Fragrance note: fresh, tart-woody, coniferous.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04088681
出典データセットuspto-grants-1978_05
ORD IDord-9a4f5dd4dae64917b167c5c127b60dfe
出典メモuspto-grants-1978_05