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Linalool → 3-(2,4-Dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl ester

HRID 1789644
ノート
印刷プレビュー

反応式

HRID 1789644 の反応式
[CH2:1]=[CH:2][C:3]([CH2:6][CH2:7][CH:8]=[C:9]([CH3:11])[CH3:10])([CH3:5])[OH:4].C(N(CC)CC)C.[OH:19][C:20]1[CH:25]=[C:24]([OH:26])[CH:23]=[CH:22][C:21]=1[CH:27]=[CH:28][C:29](O)=[O:30].CN([P+](ON1N=NC2C=CC=CC1=2)(N(C)C)N(C)C)C.F[P-](F)(F)(F)(F)F>C1COCC1.CN(C=O)C>[CH3:5][C:3]([O:4][C:29](=[O:30])[CH:28]=[CH:27][C:21]1[CH:22]=[CH:23][C:24]([OH:26])=[CH:25][C:20]=1[OH:19])([CH:2]=[CH2:1])[CH2:6][CH2:7][CH:8]=[C:9]([CH3:11])[CH3:10]
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 4

HCID 6549LinaloolHCID 8471TriethylamineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 33594933-(2,4-dihydroxyphenyl)prop-2-enoic Acid

生成物 1

HCID 669332403-(2,4-Dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl ester

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of linalool (1.74 g, 11.3 mmol) and triethylamine (2.30 g, 22.6 mmol) in anhydrous THF (150 mL) stirred for 5 min at 22° C. is added 3-(2,4-dihydroxyphenyl)-acrylic acid (2.04 g, 11.3 mmol). To this heterogeneous solution is added BOP Reagent (5.00 g, 11.3 mmol; Aldrich #22,608-4) in DMF (10 mL), and the subsequent homogeneous reaction mixture is stirred for 1 h. The reaction mixture is partitioned between ether (200 mL) and water (400 mL); the organic layer is removed and washed with ether (200 mL). The combined organic layers are washed sequentially with saturated sodium bicarbonate solution (200 mL) and brine (200 mL). The organic layer is dried over anhydrous magnesium sulfate, vacuum filtered and concentrated to give 3-(2,4-dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl ester as an oil that is purified by flash chromatography.

後処理

  1. customThe reaction mixture is partitioned between ether (200 mL) and water (400 mL)
  2. customthe organic layer is removed
  3. washwashed with ether (200 mL)
  4. washThe combined organic layers are washed sequentially with saturated sodium bicarbonate solution (200 mL) and brine (200 mL)
  5. dry with materialThe organic layer is dried over anhydrous magnesium sulfate, vacuum
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-fc60b71ab90445cab311ed1798fa62bf
出典データセット
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07071151B2

反応ノート

読み込み中…

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