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Triethylborane → 3-Chloro-5-ethylbenzaldehyde

HRID 1503801
ノート
印刷プレビュー

反応式

HRID 1503801 の反応式
P([O-])([O-])([O-])=O.[K+].[K+].[K+].C(B([CH2:14][CH3:15])CC)C.Br[C:17]1[CH:18]=[C:19]([CH:22]=[C:23]([Cl:25])[CH:24]=1)[CH:20]=[O:21]>C1COCC1.CCOC(C)=O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:25][C:23]1[CH:22]=[C:19]([CH:18]=[C:17]([CH2:14][CH3:15])[CH:24]=1)[CH:20]=[O:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 7357TriethylboraneHCID 62657Potassium Phosphate, TribasicHCID 177509523-Bromo-5-chlorobenzaldehyde

生成物 1

HCID 840830783-Chloro-5-ethylbenzaldehyde収率 42.9%

試薬・触媒・溶媒 3

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒
HCID 8028
Tetrahydrofuran
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

PdCl2(dppf) (37 mg, 0.046 mmol), potassium phosphate (1.93 g, 9.11 mmol) and triethylborane (1M in hexane, 0.45 g, 4.56 mmol) were added to a solution of 3-bromo-5-chloro-benzaldehyde (1.0 g, 4.56 mmol) in THF (20 mL) at ambient temperature and the mixture was refluxed for 12 h. The reaction mixture was brought to ambient temperature, diluted with EtOAc and washed with water. The organic layer was dried (Na2SO4), filtered, concentrated and the residue was purified by column chromatography on silica (100-200 mesh) eluting with 2% EtOAc in petroleum ether to afford the title compound (330 mg, 41%) as a pale yellow liquid: 1H NMR (400 MHz, DMSO-d6) δ 9.97 (s, 1H), 7.75 (d, J=1.6 Hz 1H), 7.73 (s, 1H), 7.65 (s, 1H), 2.74-2.68 (m, 2H), 1.23 (t, J=7.6 Hz, 3H); ESIMS m/z 168.0 ([M]+); IR (thin film) 3071, 1699, 692 cm−1.

後処理

  1. temperaturethe mixture was refluxed for 12 h
  2. customwas brought to ambient temperature
  3. washwashed with water
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customthe residue was purified by column chromatography on silica (100-200 mesh)
  8. washeluting with 2% EtOAc in petroleum ether

出典と根拠

ORDレコード
ord-db80a8333a1c4a57a4fae3b0bb34a8bb
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09212164B2

反応ノート

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