3-Fluorophenol → HCID 13039288、化合物

HRID 851050ノート

反応式

HRID 851050 の反応式
[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C@@H:9]([OH:12])[C@H:8]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:7]1)=[O:5])[CH3:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:38][C:39]1[CH:40]=[C:41](O)[CH:42]=[CH:43][CH:44]=1.N(C(OCC)=O)=NC(OCC)=O>C1C=CC=CC=1.CCOCC>[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C@H:9]([O:12][C:43]2[CH:42]=[CH:41][CH:40]=[C:39]([F:38])[CH:44]=2)[C@H:8]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH2:7]1)=[O:5])[CH3:2]

参加物

7

反応物 4

HCID 97433-FluorophenolHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 13039299HCID 13039299、化合物

生成物 1

HCID 13039288HCID 13039288、化合物

試薬・触媒・溶媒 2

HCID 241Benzene溶媒2 回HCID 3283Diethyl Ether溶媒

実験手順

To a mixture of 6.23 g of trans-1-ethoxycarbonyl-3-phenyl-4-piperidinol, 7.21 g of triphenylphosphine and 2.49 ml of m-fluorophenol in 250 ml of anhydrous benzene is added dropwise under nitrogen at 5° C. over a 90 minute period a solution of 4.79 g of diethyl azodicarboxylate in 250 ml of benzene. After the addition is complete the mixture is stirred overnight at room temperature. The solid is filtered, washed with benzene, and the filtrate is concentrated in vacuo to a gum. The gum is triturated overnight in a stoppered flask with 250 ml of hexane. The solid is filtered and washed with hexane. The filtrate is washed with 10% aqueous sodium hydroxide solution (3×75 ml), water (2×100 ml), saturated sodium chloride solution (100 ml) and dried overnight over anhydrous sodium sulfate. Filtration and concentration in vacuo affords a light yellow oil. Chromatography of the oil on 430 g of silica gel, using 2:1 (petroleum ether:ether), affords a colorless, cloudy gum. Trituration of the gum with petroleum ether yields product as a colorless crystalline solid, mp 74°-76.5° C.

後処理

  1. additionAfter the addition
  2. filtrationThe solid is filtered
  3. washwashed with benzene
  4. concentrationthe filtrate is concentrated in vacuo to a gum
  5. customThe gum is triturated overnight in a stoppered flask with 250 ml of hexane
  6. filtrationThe solid is filtered
  7. washwashed with hexane
  8. washThe filtrate is washed with 10% aqueous sodium hydroxide solution (3×75 ml), water (2×100 ml), saturated sodium chloride solution (100 ml)
  9. dry with materialdried overnight over anhydrous sodium sulfate
  10. filtrationFiltration and concentration in vacuo
  11. customaffords a light yellow oil
  12. customaffords a colorless, cloudy gum

出典と根拠

ORDレコード
ord-3c9e4e92645c432fab4c27fb806ea2e2
出典データセット
uspto-grants-1983_05
特許番号
US04382141

反応ノート

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