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Hydrochloric Acid → 1-Hydroxy-4-cyclopropanecarbonyloxy-2,2,6,6-tetramethylpiperidine hydrochloride

HRID 2117391
ノート
印刷プレビュー

反応式

HRID 2117391 の反応式
[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([O:10][C:11]([CH:13]2[CH2:15][CH2:14]2)=[O:12])[CH2:4][C:3]1([CH3:17])[CH3:16].[ClH:18]>C(O)C>[ClH:18].[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([O:10][C:11]([CH:13]2[CH2:14][CH2:15]2)=[O:12])[CH2:4][C:3]1([CH3:17])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 10131000Ot-551

生成物 1

HCID 114828181-Hydroxy-4-cyclopropanecarbonyloxy-2,2,6,6-tetramethylpiperidine hydrochloride

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

The nitroxide of Example 5a (2.2 g, 9.15 mmol) was added to a solution of saturated hydrogen chloride in ethanol (20 mL). The red color disappeared quickly and the resulting yellow colored solution was boiled to give clear colorless solution. The solution was concentrated in vacuo, dissolved in 100 mL ethyl acetate and was washed with saturated NaHCO3 to obtain the hydroxylamine free-base. The ethyl acetate layer was separated, acidified with ethereal HCl, and concentrated to give white solid, which was recrystallized from ethanol (10 mL) as a white crystalline solid 1.15 g (4.13 mmol, 45.1%). m.p. 224-228° C. (dec.).

後処理

  1. customto give clear colorless solution
  2. concentrationThe solution was concentrated in vacuo
  3. dissolutiondissolved in 100 mL ethyl acetate
  4. washwas washed with saturated NaHCO3

出典と根拠

ORDレコード
ord-82a6fc9851444e93837045d26df9de36
出典データセット
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07442711B2

反応ノート

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