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HRID 2302097作成日:2026年10月27日

Butanedione → 1-Acetyl-3,5-dimethyl Adamantane

https://huagongshe.com/reaction/2302097

反応式

関与物質

役割名称HCID仕込み量
反応物ButanedioneHCID 650—
反応物N-HydroxyphthalimideHCID 10665—
反応物1,3-DimethyladamantaneHCID 12800—
反応物1,3-Diacetyl-5,7-dimethyladamantaneHCID 12113141—
反応物1-Acetyl-3,5-dimethyl-7-adamantanolHCID 13464074—
触媒Cobalt diacetateHCID 6277—
溶媒Acetic AcidHCID 176—
生成物3,5-Dimethyl-1-adamantanolHCID 2657937%
生成物1-Acetyl-3,5-dimethyl AdamantaneHCID 1211312419%
生成物1,3-Dimethyl-4-adamantanoneHCID 126443323%

反応手順

The procedure of Example 7 was repeated, except that a mixture further comprising 0.3 mmol of N-hydroxyphthalimide in addition to the 1,3-dimethyladamantane, biacetyl, cobalt(II) acetate, and acetic acid was subjected to the reaction. As a result, 1-acetyl-3,5-dimethyladamantane (yield 19%, selectivity 53%), 1,3-diacetyl-5,7-dimethyladamantane (trace), 1-acetyl-3,5-dimethyl-7-adamantanol (trace), 1,3-dimethyl-5-adamantanol (yield 7%, selectivity 19%), and 1,3-dimethyl-4-adamantanone (yield 3%, selectivity 8%) were formed, at a conversion rate from 1,3-dimethyladamantane of 36%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06429314B1
出典データセットuspto-grants-2002_08
ORD IDord-7dc3b844d7944b67a5ce8404f73c1435
出典メモuspto-grants-2002_08