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4-Bromo-3-methoxybenzoic acid → 4-Ethyl-3-methoxybenzoic acid

HRID 2204184
ノート
印刷プレビュー

反応式

HRID 2204184 の反応式
Br[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[O:11][CH3:12].[Zn](CC)[CH2:14][CH3:15]>O1CCOCC1.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]>[CH2:14]([C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[O:11][CH3:12])[CH3:15]
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 2

HCID 162158674-Bromo-3-methoxybenzoic acidHCID 178418750HCID 178418750、化合物

生成物 1

HCID 299406594-Ethyl-3-methoxybenzoic acid

試薬・触媒・溶媒 2

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒HCID 312751,4-Dioxane溶媒

反応条件

温度
70 °C

実験手順

A mixture of 4-bromo-3-methoxy-benzoic acid (2.49 g, 10.9 mmol) and Pd(dppf)Cl2 (158 mg, 0.216 mmol) were stirred in dioxane (25 mL) and Et2Zn (22 mL, 1 M in hexanes, 22 mmol) was added. The reaction mixture was heated at 70° C. for 1 h. The mixture was cooled to room temperature and was quenched with MeOH (1.1 mL). The solution was diluted with ethyl acetate (20 mL) and was washed with 1 N HCl (10 mL). The combined organics were washed with brine, dried over sodium sulfate and evaporated to dryness to give 4-ethyl-3-methoxybenzoic acid. ESI-MS m/z calc. 180.1, found 179.1 (M−1)−; Retention time: 1.77 minutes (3 min run).

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. customwas quenched with MeOH (1.1 mL)
  3. additionThe solution was diluted with ethyl acetate (20 mL)
  4. washwas washed with 1 N HCl (10 mL)
  5. washThe combined organics were washed with brine
  6. dry with materialdried over sodium sulfate
  7. customevaporated to dryness

出典と根拠

ORDレコード
ord-d6998c2e29e4440c821fa70f70a40d39
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365588B2

反応ノート

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