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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354299생성일: 2026년 10월 25일

Triphenylphosphine → 4-[1-(Tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzene

https://huagongshe.com/reaction/354299

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-Iodo-2-methylphenolHCID 143713—
반응물(S)-(-)-N-Boc-prolinolHCID 643448—
반응물Diisopropyl azodicarboxylateHCID 5363146—
용매TetrahydrofuranHCID 8028—
생성물4-[1-(Tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzeneHCID 2351244778%

반응 조건

온도70 °C

반응 단계

To a stirred solution of 4-iodo-2-methylphenol (465 mg, 1.987 mmol), N-tert-butoxycarbonylprolinol (400 mg, 1.987 mmol), and Ph3P (625 mg, 2.384 mmol) in THF (7 mL) was added dropwise DIAD (0.5 mL, 2.404 mmol) at room temp, and the mixture was stirred for 13 hr at 70° C. The reaction mixture was concentrated in vacuo and the residue was chromatographed on silica-gel with n-hexane-EtOAc (9:1, v/v) as eluent to give 645.3 mg (78%) 4-[1-(tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzene as a pale yellow oil. 1H-NMR (400 MHz, CDCl3) δ1.47 (s, 9H), 1.83-1.89 (m, 1H), 1.96-2.04 (m, 3H), 2.16 (s, 3H), 3.37-3.43 (br m, 2H), 3.81, 3.94 (br m each, 1H), 4.08-4.18 (m, 2H), 6.62 (br s, 1H), 7.42 (s, 2H); MS (FAB) m/z 418 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756378B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-237852e4b0de4b2bba8c32fbe85e796c
출처 메모uspto-grants-2004_06