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硼11三氟化硼气体 → HCID 58550953,化合物

HRID 1908013
笔记
打印预览

反应方程式

HRID 1908013 反应方程式
[CH:1]([O:8][CH2:9][CH3:10])([O:5][CH2:6][CH3:7])OCC.B(F)(F)F.[O:15]=[C:16]1[C:40]2[C:35](=[CH:36][CH:37]=[CH:38][CH:39]=2)[O:34][C:18]2([CH2:23][CH2:22][N:21]([C:24]([O:26][CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[O:25])[CH2:20][CH2:19]2)[CH2:17]1.C(N(C(C)C)C(C)C)C>ClCCl>[CH2:9]([O:8][CH:1]([O:5][CH2:6][CH3:7])[CH:17]1[C:18]2([CH2:23][CH2:22][N:21]([C:24]([O:26][CH2:27][C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)=[O:25])[CH2:20][CH2:19]2)[O:34][C:35]2[C:40](=[CH:39][CH:38]=[CH:37][CH:36]=2)[C:16]1=[O:15])[CH3:10]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

6

反应物 4

HCID 6356硼11三氟化硼气体HCID 31214原甲酸三乙酯HCID 81531N,N-二异丙基乙胺HCID 30561364Benzyl 4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate

产物 1

HCID 58550953HCID 58550953,化合物收率 78.7%

试剂、催化剂与溶剂 1

HCID 6344二氯甲烷溶剂3 次

反应条件

温度
0 °C

实验过程

To a solution of triethyl orthoformate (71 mL, 0.43 mol)] in dichloromethane (250 mL) at −10° C. under nitrogen was added boron trifluoride diethyletherate (54 mL, 0.43 mol) dropwise over 30 minutes. The mixture was allowed to warm to 0° C. and stirring was continued at 0° C. for 15 minutes. The mixture was then cooled to −78° C. and a solution of benzyl 4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate (50 g, 0.14 mol) in dichloromethane (250 mL) was added dropwise over 1 hour, followed by N-ethyl-N-isopropylpropan-2-amine (87 mL, 0.50 mol) over 1 hour at −78° C. The mixture was continued to stir at −78° C. for 30 minutes and then at 25° C. for 15 hours. The reaction mixture was diluted with dichloromethane (750 mL) and then partitioned with saturated sodium bicarbonate solution (500 mL). The organic phase was washed with water (500 mL), saturated sodium chloride solution (500 mL), dried over magnesium sulfate and concentrated under reduced pressure. Purification by silica gel flash chromatography (0-50% ethyl acetate in hexane) afforded benzyl 3-(diethoxymethyl)-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate (50 g, 78%) as a yellow oil. ESI-MS m/z calc. 453.2. found 408.5 (M+1-OEt)+; Retention time: 2.08 minutes (3 min run).

后处理

  1. temperatureThe mixture was then cooled to −78° C.
  2. stirringto stir at −78° C. for 30 minutes
  3. waitat 25° C. for 15 hours
  4. custompartitioned with saturated sodium bicarbonate solution (500 mL)
  5. washThe organic phase was washed with water (500 mL), saturated sodium chloride solution (500 mL)
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customPurification by silica gel flash chromatography (0-50% ethyl acetate in hexane)

来源与证据

ORD记录
ord-30de73e6098d455cb692851748d54488
来源数据集
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08598164B2

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记