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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1630968생성일: 2026년 10월 26일

Sodium borohydride → (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol

https://huagongshe.com/reaction/1630968

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehydeHCID 23091101—
용매MethanolHCID 887—
용매Ammonium ChlorideHCID 25517—
생성물(5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanolHCID 5855419797%

반응 조건

온도5 °C

반응 단계

Sodium borohydride (2.2 g, 57.8 mmol) was added portion-wise into a solution of 5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde (16.3 g, 57.8 mmol) in MeOH (300 mL) cooled at 5° C. After 30 min, the reaction mixture was diluted with a saturated aqueous solution of NH4Cl (300 mL) and extracted with EtOAc (600 mL+300 mL). The organic layers were washed with a saturated aqueous solution of NH4Cl (150 mL) and brine (300 mL). The organic layers were combined, dried (MgSO4) and the solvents were removed under reduced pressure to give the title compound as a yellow oil (15.9 g, 97%) used without further purification in the next step. HPLC (Method A), Rt 2.1 min (Purity: 94.9%). UPLC/MS, M+(ESI): 284.1, 286.0. 1H NMR (CDCl3, 300 MHz) δ 7.38 (dd, J=8.5, 2.4 Hz, 1H), 7.26 (d, J=2.4 Hz, 1H), 7.13 (d, J=8.5 Hz, 1H), 6.40 (brs, 1H), 4.86 (d, J=13.9 Hz, 1H), 4.67 (d, J=13.9 Hz, 1H), 3.06-2.88 (m, 2H), 2.61 (td, J=11.4, 3.2 Hz, 1H), 1.88-1.58 (m, 4H), 1.53-1.32 (m, 2H), 0.90 (d, J=6.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791142B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-b559cc17ebc64fb9ae8e7d22fbd0cf52
출처 메모uspto-grants-2014_07