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Potassium Carbonate → 6-(4-Bromobenzyl)-2-oxa-6-aza-spiro[3.3]heptane

HRID 1505905
ノート
印刷プレビュー

反応式

HRID 1505905 の反応式
[CH2:1]1[C:4]2([CH2:7][NH:6][CH2:5]2)[CH2:3][O:2]1.[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13]Br)=[CH:11][CH:10]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.[I-].[Na+]>[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][N:6]2[CH2:7][C:4]3([CH2:3][O:2][CH2:1]3)[CH2:5]2)=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 685274-Bromobenzyl bromideHCID 231118872-Oxa-6-azaspiro[3.3]heptane

生成物 1

HCID 582664706-(4-Bromobenzyl)-2-oxa-6-aza-spiro[3.3]heptane収率 68%

試薬・触媒・溶媒 2

HCID 5238Sodium Iodide触媒HCID 8028Tetrahydrofuran
溶媒

実験手順

A mixture of 2-oxa-6-aza-spiro[3.3]heptane (˜3.72 mmol), 4-bromobenzyl bromide (0.39 g, 1.54 mmol), potassium carbonate (0.64, 4.63 mmol) and sodium iodide (11 mg, 0.08 mmol) in THF (10 mL) was stirred at ambient temperature for 16 h. The solid was removed by filtration, washed with THF and the combined filtrate was evaporated. The resultant residue was purified by flash chromatography (silica, 12 g column, ISCO, 0-100% ethyl acetate in pentane then 10% methanol in DCM) to afford the title compound (0.28 g, 68%) as a viscous oil which crystallised on standing to a pale yellow solid. 1H NMR (CDCl3, 300 MHz): 7.46-7.40 (m, 2H), 7.15-7.09 (m, 2H), 4.73 (s, 4H), 3.48 (s, 2H), 3.35 (s, 4H).

後処理

  1. customThe solid was removed by filtration
  2. washwashed with THF
  3. customthe combined filtrate was evaporated
  4. customThe resultant residue was purified by flash chromatography (silica, 12 g column, ISCO, 0-100% ethyl acetate in pentane

出典と根拠

ORDレコード
ord-d658c9ecb6f9490683db68a8587e1517
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09216980B2

反応ノート

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