三苯基膦 → Methyl 4-(4-chromanoyloxy)-2-methoxybenzoate

HRID 1682

反应方程式

HRID 1682 反应方程式
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[O:33]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[CH:36](O)[CH2:35][CH2:34]1.N(C(OCC)=O)=N[C:46](OCC)=[O:47]>C1COCC1>[O:33]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[CH:36]([C:46]([O:1][C:2]2[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=2)=[O:47])[CH2:35][CH2:34]1

参与物

6

反应物 4

HCID 11776三苯基膦HCID 928904-二乙酰醇HCID 220568偶氮二甲酸二乙酯HCID 125326764-羟基-2-甲基氧苯甲酸甲酯

产物 1

HCID 19691018Methyl 4-(4-chromanoyloxy)-2-methoxybenzoate

试剂、催化剂与溶剂 1

HCID 8028四氢呋喃溶剂2 次

反应条件

温度
0 °C

实验过程

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (364 mg, 2.0 mmol) in dry THF (1.25 mL) was added triphenylphosphine (525 mg, 2.0 mmol) and the solution was cooled to 0° C. A 500 mL volume of 4-chromanol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 mL, 2.0 mmol) in THF was added dropwise via syringe over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 92:8 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(4-chromanoyloxy)-2-methoxybenzoate.

后处理

  1. filtrationThe reaction was filtered
  2. customthe solvent was removed under reduced pressure
  3. customThe residue was chromatographed on a silica gel column
  4. washEtOAc and eluted with same
  5. customthe solvent removed under reduced pressure

来源与证据

ORD记录
ord-c76a22e184294ef893b6fc5df9e611d7
来源数据集
uspto-grants-1998_03
专利号
US05726172

关联笔记

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