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HRID 65522作成日:2026年10月24日

1-Butanamine, N,N-dibutyl-, hydrochloride (1:1) → 3,4-Bis(p-toluyloxy)-alpha-[(tert-butylamino)methyl]benzyl alcohol

https://huagongshe.com/ja/reaction/65522

反応式

関与物質

役割名称HCID仕込み量
反応物1-Butanamine, N,N-dibutyl-, hydrochloride (1:1)HCID 80570—
反応物Sodium borohydrideHCID 4311764—
反応物3,4-bis(p-toluyloxy)phenyl N-(tert-butyl)aminomethyl ketone hydrochlorideHCID 70467733—
生成物3,4-Bis(p-toluyloxy)-alpha-[(tert-butylamino)methyl]benzyl alcoholHCID 2131997590%

反応手順

The crude products of the foregoing examples containing minor amounts of acid-acceptor amine hydrochloride can be used without further purification in the reduction step to produce the corresponding phenylethanolamine compound. For example, a sample of 3,4-bis(p-toluyloxy)phenyl N-(tert-butyl)aminomethyl ketone hydrochloride containing about 6 percent of tributylamine hydrochloride was reduced with sodium borohydride to give 3,4-bis(p-toluyloxy)-α-[(tert-butylamino)methyl]benzyl alcohol (bitolterol) in greater than 90% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04614830
出典データセットuspto-grants-1986_09
ORD IDord-4380dbd7b8154b2390a8d98f80cae45b
出典メモuspto-grants-1986_09