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HRID 1702964作成日:2026年10月25日

Acetyl chloride → Succinate

https://huagongshe.com/reaction/1702964

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物Succinyl chlorideHCID 10970—
反応物Pentanedioyl dichlorideHCID 17887—
反応物BruceolideHCID 99531—
反応物Methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylateHCID 12302104—
生成物SuccinateHCID 160419—
生成物Glutarate(2-)HCID 4418048—
生成物3,5-Dioxohexanoic acidHCID 5459844—

反応手順

In accordance with the above procedure, but where, in place of 3,4-dimethyl-2-pentenoyl chloride, there is utilized benzoyl chloride, trimethoxybenzoyl chloride or cinnamoyl chloride there is obtained the corresponding 3-ester or 3,15-diester. Similarly, but where, in place of bruceolide, there is utilized brusatol and as an acid chloride there is utilized succinoyl chloride, glutaroyl chloride and acetyl chloride, there is obtained 3,3-bisbrusatolyl succinate, 3,3-bisbrusatolyl glutarate and 3,11,12-brusatolyl triacetate, 3, 11, 12 bis brusatolyl triacetate can also be prepared by acetylation with pyridine in acetic anhydride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04350638
出典データセットuspto-grants-1982_09
ORD IDord-233cfa63431c469c810679ed744ad36f
出典メモuspto-grants-1982_09