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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12586생성일: 2026년 10월 23일

Hydrochloric Acid → (R)-2-tert-butoxycarbonylamino-4-(4-heptyloxy-phenyl)-2-methyl-butyric acid

https://huagongshe.com/ko/reaction/12586

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Methyl-2-buteneHCID 10553—
반응물Sodium ChloriteHCID 23668197—
반응물[(R)-1-Formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 59339517—
용매tert-ButanolHCID 6386—
용매Ethyl AcetateHCID 8857—
용매Monobasic potassium phosphateHCID 516951—
생성물(R)-2-tert-butoxycarbonylamino-4-(4-heptyloxy-phenyl)-2-methyl-butyric acidHCID 58897679—

반응 단계

To a stirred solution of [(R)-1-formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester (103 mg, 0.26 mMol) in tert-butanol (1 ml) and 10% aqueous KH2PO4 (1 ml) is added 2-methyl-2-butene (0.66 ml, 5.27 mMol) and sodium chlorite (59 mg, 0.52 mMol). The mixture is stirred at RT for 1 hour. The reaction mixture is then poured onto a biphasic mixture of AcOEt and HCl (aqueous, 1M). The aqueous phase is extracted twice with AcOEt. The combined organic layers are washed with a small amount of NaHCO3 (saturated aqueous solution), dried (Na2SO4) and concentrated under reduced pressure. Column chromatography eluting with 5% MeOH in CH2Cl2 gives the title compound as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728020B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ed19de40aa354320974dd94b4cf5e358
출처 메모uspto-grants-2010_06