1-(4-Fluorophenyl)piperazine → Piperazine, 1-(1,4-dioxaspiro[4.5]dec-8-yl)-4-(4-fluorophenyl)-

HRID 432600ノート

反応式

HRID 432600 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[CH2:14]1[O:24][C:17]2([CH2:22][CH2:21][C:20](=O)[CH2:19][CH2:18]2)[O:16][CH2:15]1>C(Cl)CCl>[O:16]1[C:17]2([CH2:22][CH2:21][CH:20]([N:11]3[CH2:12][CH2:13][N:8]([C:5]4[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=4)[CH2:9][CH2:10]3)[CH2:19][CH2:18]2)[O:24][CH2:14][CH2:15]1

参加物

4

反応物 2

HCID 752601-(4-Fluorophenyl)piperazineHCID 5674151,4-Dioxaspiro[4.5]decan-8-one

生成物 1

HCID 18760058Piperazine, 1-(1,4-dioxaspiro[4.5]dec-8-yl)-4-(4-fluorophenyl)-

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

A mixture of 11.5 gm of 1-(4-fluoro-phenyl)-piperazine 10.0 gm of 1,4-cyclohexanedione mono-ethylene ketal (available from Aldrich) and 27.2 gm NaB(OAc)3 in 250 ml dichloroethylene was kept for 18 hours at ambient temperature. The solvents were removed and the residue partitioned between ethyl acetate (200 ml) and 2N NaOH (200 ml). The ethyl acetate layer is washed with 2×20 ml water and dried over Na2SO4. The crude 1-(1,4-dioxa-spiro[4.5]dec-8-yl)-4-(4-fluoro-phenyl)-piperazine (20.1 gm of a solid) obtained after removing the solvents had a melting point of 116-118° C. A sample of this material (C18H25FN2O2) showed an elemental analysis of C, 67.24%, H, 8.22%. N, 8.98%.

後処理

  1. customThe solvents were removed
  2. customthe residue partitioned between ethyl acetate (200 ml) and 2N NaOH (200 ml)
  3. washThe ethyl acetate layer is washed with 2×20 ml water
  4. dry with materialdried over Na2SO4

出典と根拠

ORDレコード
ord-fcf6662ea1e0437584edb0211fe6b6ee
出典データセット
uspto-grants-2003_12
特許番号
US06664258B1

反応ノート

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