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Triethylborane → Methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate

HRID 2177144
ノート
印刷プレビュー

反応式

HRID 2177144 の反応式
Br[C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH:5]=[CH:6][C:7]=1[OH:8].C([O-])([O-])=O.[Cs+].[Cs+].[CH2:21](B(CC)CC)[CH3:22]>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].O1CCCC1>[CH2:21]([C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH:5]=[CH:6][C:7]=1[OH:8])[CH3:22]
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

6

反応物 3

HCID 7357TriethylboraneHCID 10796Cesium carbonateHCID 22558720Methyl 3-(3-bromo-4-hydroxyphenyl)propanoate

生成物 1

HCID 90418287Methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate

試薬・触媒・溶媒 2

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

反応条件

温度
65 °C

実験手順

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed methyl 3-(3-bromo-4-hydroxyphenyl)propanoate (220 mg, 0.85 mmol, 1.00 equiv), Pd(dppf)Cl2 (25.76 mg, 0.04 mmol, 0.04 equiv), Cs2CO3 (616.4 mg), tetrahydrofuran (5 mL), triethylborane (1.26 mL). The resulting solution was stirred overnight at 65° C. in an oil bath. The reaction was then quenched by the addition of 5 mL of water. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 20 mL of EA. The resulting mixture was washed with 3×10 mL of H2O. The mixture was dried over anhydrous sodium sulfate. The residue was applied onto a silica gel column with ethylacetate/petroleum ether (10:90). This resulted in 300 mg (170%) of methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate as colorless oil.

後処理

  1. customInto a 50-mL round-bottom flask purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. customThe reaction was then quenched by the addition of 5 mL of water
  4. concentrationThe resulting mixture was concentrated under vacuum
  5. additionThe resulting solution was diluted with 20 mL of EA
  6. washThe resulting mixture was washed with 3×10 mL of H2O
  7. dry with materialThe mixture was dried over anhydrous sodium sulfate
  8. customThis resulted in 300 mg (170%) of methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate as colorless oil

出典と根拠

ORDレコード
ord-a5ce451417444c5caeb8f3921e094aef
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09067898B1

反応ノート

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