Dimethylamine → HCID 22349540、化合物

HRID 1517517ノート

反応式

HRID 1517517 の反応式
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][C:8]2=O)=[CH:4][CH:3]=1.[CH3:12][NH:13][CH3:14].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][CH:8]2[N:13]([CH3:14])[CH3:12])=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 674DimethylamineHCID 1397781-Indanone, 6-bromo-HCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 22349540HCID 22349540、化合物

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

反応条件

温度
120 °C

実験手順

(Method 1): 6-Bromo-indan-1-one (0.23 mmol) and dimethyl-amine (0.71 mmol) were mixed in 3 ml of 1,2-dichloroethane in a process vial, which was sealed with a septum. Sodium triacetoxyborohydride (0.47 mmol) was added under argon atmosphere. The suspension was subjected to microwave irradiating conditions (CEM Discover® equipped with a CEM Explorer® automated reaction handling module). The reaction mixture was heated for 5 min at 120° C. and then cooled. The crude was evaporated to dryness and then suspended in aqueous NaHCO3 The product was extracted with CH2Cl2 and washed with aqueous NaHCO3. The CH2Cl2 extract was dried with anhydrous Na2SO4, filtered and evaporated to dryness to give the crude product (6-bromo-indan-1-yl)-dimethyl-amine. The crude was purified by flash column chromatography (CH2Cl2-MeOH as eluents) by using a CombiFlash Companion™ system to yield the title compound (85%). MS [MH]+=240.

後処理

  1. customwhich was sealed with a septum
  2. customto microwave irradiating conditions (CEM Discover®
  3. customequipped with a CEM Explorer®
  4. customreaction handling module)
  5. temperaturecooled
  6. customThe crude was evaporated to dryness
  7. extractionwas extracted with CH2Cl2
  8. washwashed with aqueous NaHCO3
  9. extractionThe CH2Cl2 extract
  10. dry with materialwas dried with anhydrous Na2SO4
  11. filtrationfiltered
  12. customevaporated to dryness

出典と根拠

ORDレコード
ord-fb7954f790ac4c7aba73286c7db9d416
出典データセット
uspto-grants-2012_07
特許番号
US08232307B2

反応ノート

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