돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 889972생성일: 2026년 10월 26일

Methyl iodide → 1-Methyl-4-(4-nitro-benzyl)-1,2,3,6-tetrahydro-pyridine

https://huagongshe.com/reaction/889972

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물4-(4-Nitrobenzyl)pyridineHCID 14129—
반응물Sodium HydroxideHCID 14798—
촉매Tetrabutylammonium IodideHCID 67553—
용매DichloromethaneHCID 6344—
생성물1-Methyl-4-(4-nitro-benzyl)-1,2,3,6-tetrahydro-pyridineHCID 22249202—

반응 단계

4-(4-Nitrobenzyl)pyridine (64 g) and TBAI (6 g) were dissolved in CH2Cl2 (500 mL) and the solution was suspended with NaOH (aq. 5N, 450 mL) in a 3L 3-necked round bottom flask. With vigorous stirring, iodomethane (213 g) was added and stirred vigorously at RT for 60 h (or until blue color disappears). The reaction was quenched with dimethylamine (100 mL) and MeOH (300 mL) and stirred for 2 h. NaBH4 (19 g) was added to the mixture in small portions. The reaction mixture was stirred for 30 min at RT, then partitioned between CH2Cl2/H2O (500 mL/500 mL). The organic layer was collected and the aqueous layer was washed with CH2Cl2 (300 mL×3). The combined organic layers was washed with brine then concentrated in vacuo. The residue was purified on a silica wash-column (7% TEA in EtOAc). The desired fractions were combined and concentrated under vacuum to give the desired compound as a dark gray solid. (MS: M+1=261).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06995162B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-0b2f43c25e1c408186354a9f71044eda
출처 메모uspto-grants-2006_02