Ethyl Acetate → (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(tetradecyloxy)furan-2-carboxylate

HRID 57211

반응식

HRID 57211 반응식
[CH2:1]([O:15][C:16]1[O:20][C:19]([C:21]([OH:23])=[O:22])=[CH:18][CH:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].C(=O)([O-])[O-].[K+].[K+].Br[CH2:31][C:32]1[O:33][C:34](=[O:38])[O:35][C:36]=1[CH3:37].CCOC(C)=O>CN(C=O)C>[CH2:1]([O:15][C:16]1[O:20][C:19]([C:21]([O:23][CH2:31][C:32]2[O:33][C:34](=[O:38])[O:35][C:36]=2[CH3:37])=[O:22])=[CH:18][CH:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 1151755-(Tetradecyloxy)-2-furoic acidHCID 107741414-(Bromomethyl)-5-methyl-1,3-dioxol-2-one

생성물 1

HCID 49869762(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(tetradecyloxy)furan-2-carboxylate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a stirred, room temperature solution of 5-(tetradecyloxy)furan-2-carboxylic acid (0.228 g, 0.70 mmol) in DMF (4 mL) was added potassium carbonate (0.146 g, 1.05 mmol) and 4-(bromomethyl)-5-methyl-1,3-dioxol-2-one (0.160 g, 0.84 mmol). The reaction vessel was capped and stirring was continued for 14 hrs at which time TLC ((20% EtOAc in Hexanes Rf=0.10 (SM) and 0.40 (Prod)) indicated complete consumption of the starting material. The reaction was quenched by the addition of water (5 mL), brine (5 mL) and EtOAc (30 mL). The biphasic mixture was transferred to a seperatory funnel and the organic phase was extracted 3 times with brine (3×10 mL). The organic phase was dried and concentrated to give a colourless oil. The resulting crude material was purified by flash chromatography eluting with 5-20% EtOAc in hexanes to yield a colourless syrup that solidified on standing. 1H NMR (400 MHz, DMSO-d6) δ: 7.2 (d, 1H), 5.6 (d, 1H), 5.1 (s, 2H), 4.1 (t, 2H), 2.18 (s, 3H), 1.6-1.8 (m, 2H), 1.3-1.4 (m, 2H), 1.23 (d, 6H), 1.2 (s, 20H), 0.85 (t, 3H).

후처리

  1. customThe reaction vessel was capped
  2. customconsumption of the starting material
  3. customThe reaction was quenched by the addition of water (5 mL), brine (5 mL) and EtOAc (30 mL)
  4. customThe biphasic mixture was transferred to a seperatory funnel
  5. extractionthe organic phase was extracted 3 times with brine (3×10 mL)
  6. customThe organic phase was dried
  7. concentrationconcentrated
  8. customto give a colourless oil
  9. customThe resulting crude material was purified by flash chromatography
  10. washeluting with 5-20% EtOAc in hexanes
  11. customto yield a colourless syrup that

출처 및 근거

ORD 기록
ord-925f62bc6a8d4fbf83dbe7638c1244f8
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09434718B2

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