1,4-Dioxaspiro[4.5]decan-8-one → 8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decane

HRID 1246272

反応式

HRID 1246272 の反応式
[Cl-].[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:5][CH:4]=1.CC(C)([O-])C.[K+].[CH2:35]1[O:45][C:38]2([CH2:43][CH2:42][C:41](=O)[CH2:40][CH2:39]2)[O:37][CH2:36]1>C1COCC1>[F:2][C:3]1[CH:4]=[CH:5][C:6]([CH:9]=[C:41]2[CH2:42][CH2:43][C:38]3([O:45][CH2:35][CH2:36][O:37]3)[CH2:39][CH2:40]2)=[CH:7][CH:8]=1

参加物

5

反応物 3

HCID 5674151,4-Dioxaspiro[4.5]decan-8-oneHCID 2733554(4-Fluorobenzyl)triphenylphosphonium chlorideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 121339508-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decane収率 79.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

To a stirring solution of 4-fluorophenylmethyl triphenylphosphonium chloride (39 g, 96 mmol, Lancaster) in 500 mL of dry THF at −78° C. was added 1 M potassium t-butoxide in THF (106 mL, 106 mmol, Aldrich). The reaction was stirred for 30 min and then warmed to 0° C. The reaction was stirred for 30 min and then 1,4-cyclohexanedione mono-ethylene ketal (15.0 g, 96 mmol, Aldrich) was added. After 30 min, the reaction was warmed to room temperature and allowed to stir overnight. The reaction was heated to reflux for 4 h and then cooled to room temperature. The reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL). The organic layer was separated, washed with brine, dried over sodium sulfate, and conc in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate) to yield 18.9 g of a colorless oil. MS (ESI) 251 (M+H).

後処理

  1. stirringThe reaction was stirred for 30 min
  2. waitAfter 30 min
  3. temperaturethe reaction was warmed to room temperature
  4. stirringto stir overnight
  5. temperatureThe reaction was heated
  6. temperatureto reflux for 4 h
  7. temperaturecooled to room temperature
  8. customThe reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL)
  9. customThe organic layer was separated
  10. washwashed with brine
  11. dry with materialdried over sodium sulfate
  12. customThe solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate)

出典と根拠

ORDレコード
ord-154ae93b150c458bb7c1ae76a8ea994c
出典データセット
uspto-grants-2006_10
特許番号
US07126010B2

関連ノート

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