氢氧化钾 → 3-Fluoro-4-(oxetan-3-yloxy)benzoic acid

HRID 1908106笔记

反应方程式

HRID 1908106 反应方程式
[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH:13]1[CH2:16][O:15][CH2:14]1)[C:5]([O:7]C)=[O:6].[OH-].[K+]>CO>[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH:13]1[CH2:14][O:15][CH2:16]1)[C:5]([OH:7])=[O:6]

参与物

4

反应物 2

HCID 14797氢氧化钾HCID 58550731Methyl 3-fluoro-4-(oxetan-3-yloxy)benzoate

产物 1

HCID 566044493-Fluoro-4-(oxetan-3-yloxy)benzoic acid

试剂、催化剂与溶剂 1

HCID 887(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮溶剂

实验过程

Crude methyl 3-fluoro-4-(oxetan-3-yloxy)benzoate from Step 1, MeOH (1 mL), and KOH (4.0 mL of 3.0 M, 12 mmol) were combined and the mixture was allowed to stir for 3 h at rt. The mixture was extracted with EtOAc and the organic layer was discarded. The aqueous layer was then treated with 1N HCl and the pH was adjusted to pH 3. The aqueous layer was extracted with EtOAc (3×) and the combined organic layers were dried over sodium sulfate and the solvent was removed. The crude acid was used without further purification. ESI-MS m/z calc. 212.1. found 213.0 (M+1)+; Retention time: 1.65 minutes (4 min run).

后处理

  1. extractionThe mixture was extracted with EtOAc
  2. additionThe aqueous layer was then treated with 1N HCl
  3. extractionThe aqueous layer was extracted with EtOAc (3×)
  4. dry with materialthe combined organic layers were dried over sodium sulfate
  5. customthe solvent was removed
  6. customThe crude acid was used without further purification
  7. customRetention time: 1.65 minutes (4 min run)

来源与证据

ORD记录
ord-5dbcc214258a46c985cdbfb868cdd918
来源数据集
uspto-grants-2013_12
专利号
US08598164B2

反应笔记

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