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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2046714생성일: 2026년 10월 25일

tert-Butyl acrylate → (E)-3-{1'-Methyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/2046714

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acrylateHCID 15458—
반응물(E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl esterHCID 52952087—
반응물6-Bromo-1'-methylspiro[chroman-2,4'-piperidin]-4-oneHCID 57720805—
생성물(E)-3-{1'-Methyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid tert-butyl esterHCID 52952512—

반응 단계

(E)-3-{1′-Methyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid tert-butyl ester was synthesized starting from 1′-methyl-6-bromo-spiro[chromane-2,4′-piperidine]-4-one (1.62 g, 5.22 mmol) according to the procedure for preparation of Intermediate 1, Step B, using tert-butylacrylate, giving a yellow solid (1.45 g). The resulting product was dissolved in a 20% TFA/DCM mixture (25 ml) and stirred at RT. After 16 h, the solvent was evaporated and the residue was partitioned between DCM and a saturated NaHCO3 solution. Then the aqueous phase was acidified with a 6 M solution of HCl and evaporated. The residue was suspended in a 9:1 DCM/MeOH mixture (70 ml) and the insoluble salts were filtered off. The solvent was dried over Na2SO4 and evaporated, giving (E)-3-{1′-methyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (890 mg) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08592444B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-fcc8e2b1a33a4d8783039c6afe3399ca
출처 메모uspto-grants-2013_11