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HRID 2076791作成日:2026年10月26日

[(R)-1-hydroxymethyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester → [(R)-1-Formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2076791

反応式

関与物質

役割名称HCID仕込み量
反応物[(R)-1-hydroxymethyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 12964546—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物[(R)-1-Formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 59339517—

反応手順

To a stirred solution of [(R)-1-hydroxymethyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester (1.98 g, 5.03 mMol) in CH2Cl2 (20 ml) is added N-morpholine-N-oxide (884 mg, 7.54 mMol) and tetra-n-propylammonium perruthenate (177 mg, 0.50 mMol). The mixture is stirred at RT for 1 hour. The mixture is then filtered over a short pad of SiO2 eluting with diethyl ether. The filtrate is concentrated under reduced pressure to give the title compound. The crude product is sufficiently pure to be used in the next stage without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07928093B2
出典データセットuspto-grants-2011_04
ORD IDord-fa685990a6b84e969e37a0c79d408314
出典メモuspto-grants-2011_04