戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1701631作成日:2026年10月27日

9-Octadecenoyl chloride → 3-(9-Octadecenoyloxy)-4-(nicotinoyloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1701631

反応式

関与物質

役割名称HCID仕込み量
反応物9-Octadecenoyl chlorideHCID 66987—
反応物Phenolate SodiumHCID 4445035—
反応物Sodium MethoxideHCID 10942334—
反応物3-Hydroxy-4-(nicotinoyloxy)phenyl tert-butylaminomethyl ketoneHCID 20535349—
生成物3-(9-Octadecenoyloxy)-4-(nicotinoyloxy)phenyl tert-butylaminomethyl ketoneHCID 54520805—

反応手順

Following a procedure similar to that described in Example 2A above, when 3-hydroxy-4-(nicotinoyloxy)phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is reacted with 9-octadecenoyl chloride there is obtained 3-(9-octadecenoyloxy)-4-(nicotinoyloxy)phenyl tert-butylaminomethyl ketone which reacts with methanesulfonic acid to yield the methanesulfonate salt. When this methanesulfonate is reduced with sodium borohydride using the procedure described above in Example 30C, there is obtained 3-(9-octadecenoyloxy)-4-(nicotinoyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol methanesulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE030241
出典データセットuspto-grants-1980_03
ORD IDord-b11ea9828e70414eb1d8fe253626f511
出典メモuspto-grants-1980_03