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Hydrochloric Acid → HCID 66643896、化合物

HRID 1474292
ノート
印刷プレビュー

反応式

HRID 1474292 の反応式
[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9]Br.C(OC)(=O)[CH2:12][C:13]([O:15]C)=[O:14].[H-].[Na+].Cl>>[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][CH2:12][C:13]([OH:15])=[O:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 7943Dimethyl malonateHCID 24758Sodium hydrideHCID 441817992-Bromo-1-(bromomethyl)-3-fluorobenzene

生成物 1

HCID 66643896HCID 66643896、化合物

反応条件

温度
0 °C

実験手順

To a flask charged with 2-bromo-1-(bromomethyl)-3-fluorobenzene (2.0 g, 7.5 mmol) and a stir bar was added dimethyl malonate (20.0 mL, 174 mmol). The solution was cooled to 0° C. in an ice bath. To this solution was carefully added sodium hydride (0.597 g, 14.9 mmol) in small portions. When the addition was done, the reaction was kept stirring for another 30 minutes. The reaction was quenched with NH4Cl, extracted with EtOAc, washed with brine, dried over Na2SO4, and concentrated. The residue was dissolved in acetic acid (50 mL). To this solution was added HCl (50 ml, 330 mmol), and the reaction was heated to reflux for 16 hours. Analysis by LC showed formation of the desired acid. Most of the solvent was removed on a rotary evaporator. The remaining solution was diluted with 50 mL of water, and extracted with ether (50 mL×3). The extracts were combined, and washed with 1N NaOH (50 mL×2). At that point, all the acid was in the aqueous as the salt. The aqueous washes were combined, acidified, and back extracted with DCM (100 mL×2). The extracts were combined, dried over Na2SO4, and concentrated to afford 3-(2-bromo-3-fluorophenyl)propanoic acid.

後処理

  1. additionWhen the addition
  2. customThe reaction was quenched with NH4Cl
  3. extractionextracted with EtOAc
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in acetic acid (50 mL)
  8. temperaturethe reaction was heated
  9. temperatureto reflux for 16 hours
  10. customMost of the solvent was removed on a rotary evaporator
  11. additionThe remaining solution was diluted with 50 mL of water
  12. extractionextracted with ether (50 mL×3)
  13. washwashed with 1N NaOH (50 mL×2)
  14. extractionback extracted with DCM (100 mL×2)
  15. dry with materialdried over Na2SO4
  16. concentrationconcentrated

出典と根拠

ORDレコード
ord-1755c098e4764a38bab9c7d84bbe8209
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018211B2

反応ノート

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