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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2076791생성일: 2026년 10월 26일

[(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

반응식

참여 물질

역할이름HCID투입량
반응물[(R)-1-hydroxymethyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 12964546—
촉매HCID 178419074HCID 178419074—
용매DichloromethaneHCID 6344—
생성물[(R)-1-Formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 59339517—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07928093B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-fa685990a6b84e969e37a0c79d408314
출처 메모uspto-grants-2011_04