戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1156685作成日:2026年10月26日

Phenoxyacetyl chloride → 3-Hydroxy-4-(phenoxyacetoxy)phenyl isopropylaminomethyl ketone

https://huagongshe.com/reaction/1156685

反応式

関与物質

役割名称HCID仕込み量
反応物Phenoxyacetyl chlorideHCID 69703—
反応物Isoproterenone hydrochlorideHCID 2830496—
生成物3-Hydroxy-4-(phenoxyacetoxy)phenyl isopropylaminomethyl ketoneHCID 53690513—

反応手順

Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and phenoxyacetyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(phenoxyacetoxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(phenoxyacetoxy)-alpha-(isopropylaminomethyl)benzyl alcohol methanesulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04336400
出典データセットuspto-grants-1982_06
ORD IDord-8d10ca0cf045458aac95ffa20d37d498
出典メモuspto-grants-1982_06