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Formaldehyde → 4-(3-Bromophenyl)-1-methylpiperidine

HRID 1888454
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HRID 1888454 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]2[CH2:13][CH2:12][N:11]([C:14](OC(C)(C)C)=O)[CH2:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1.C=O>C(O)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]2[CH2:13][CH2:12][N:11]([CH3:14])[CH2:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 712FormaldehydeHCID 40425223tert-Butyl 4-(3-bromophenyl)piperidine-1-carboxylate

생성물 1

HCID 534078424-(3-Bromophenyl)-1-methylpiperidine수율 99.3%

시약·촉매·용매 1

HCID 284Formic Acid용매

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온도
150 °C

실험 절차

A mixture of 4-(3-bromophenyl)-1-N-Boc piperidine (430 mg, 1.26 mmol), formic acid (5 mL) and formaldehyde (0.5 mL) was heated under microwave irradiation at 150° C. for 10 minutes. The cooled reaction mixture was loaded onto a 70 g SCX-2 cartridge which was washed with methanol (200 mL) and then eluted with 2N ammonia in methanol (200 mL). Concentration of the combined basic fractions in vacuo afforded the title compound (318 mg, 99%) as a brown oil. 1H NMR (CDCl3, 300 MHz): 7.38-7.36 (m, 1H); 7.35-7.29 (m, 1H); 7.17-7.14 (m, 2H); 3.03-2.92 (m, 2H); 2.52-2.37 (m, 1H); 2.32 (s, 3H); 2.10-1.99 (m, 2H); 1.87-1.69 (m, 4H).

후처리

  1. customThe cooled reaction mixture
  2. washwas washed with methanol (200 mL)
  3. washeluted with 2N ammonia in methanol (200 mL)

출처 및 근거

ORD 기록
ord-f5eb7fe41b2043849c1e3c7136da77b3
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501765B2

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