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HRID 744791作成日:2026年10月25日

3-Benzyloxybenzyl bromide → 2(R)-isopropyl-3-(3-benzyloxyphenyl)-propanol

https://huagongshe.com/reaction/744791

反応式

関与物質

役割名称HCID仕込み量
反応物3-Benzyloxybenzyl bromideHCID 1502047—
反応物3-Acetoxy-4-tert-butylbenzyl bromideHCID 21458757—
反応物N-tert-butoxycabonyl-2(R)-methyl-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(3-hydroxyphenyl)-octanoic acid (N-butyl)-amideHCID 131719571—
溶媒Methylenechloride HexaneHCID 21226440—
生成物2(R)-isopropyl-3-(3-benzyloxyphenyl)-propanolHCID 22865734—

反応手順

The N-tert-butoxycarbonyl-2(R)-methyl-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(3-hydroxyphenyl)-octanoic acid (N-butyl)amide used as starting material is prepared analogously to Example 5a)-5l), except that in step k) instead of 3-acetoxy-4-tert-butyl-benzyl bromide there is used 3-benzyloxy-benzyl bromide, so that in step i) 2(R)-isopropyl-3-(3-benzyloxy-phenyl)-propanol, Rf (dichloromethane/hexane=1:1)=0.19, is obtained directly.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05559111
出典データセットuspto-grants-1996_09
ORD IDord-d19dc6469b77442f95cb8bb3599466b6
出典メモuspto-grants-1996_09