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1H-Benzotriazole-1-methanol → HCID 86724237、化合物

HRID 594845
ノート
印刷プレビュー

反応式

HRID 594845 の反応式
C[C:2](C)([O-:4])C.[K+].[Br:7][C:8]1[CH:9]=[C:10]2[C:18](=[CH:19][CH:20]=1)[O:17][C:13]1([CH2:16][CH2:15][CH2:14]1)[CH2:12][C:11]2=[O:21].N1([CH2:31][OH:32])C2C=CC=CC=2N=N1>C1COCC1.CCOC(C)=O>[Br:7][C:8]1[CH:9]=[C:10]2[C:18](=[CH:19][CH:20]=1)[O:17][C:13]1([CH2:14][CH2:15][CH2:16]1)[C:12]([CH2:2][OH:4])([CH2:31][OH:32])[C:11]2=[O:21]
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 2241691H-Benzotriazole-1-methanolHCID 23665647Potassium tert-butoxideHCID 667462536-Bromospiro[chroman-2,1'-cyclobutan]-4-one

生成物 1

HCID 86724237HCID 86724237、化合物収率 104.8%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 8857
Ethyl Acetate
溶媒

実験手順

A solution of potassium tert-butoxide (441 mg, 3.93 mmol) in THF (5 mL) was added to a suspension of 6-bromospiro[chromene-2,1′-cyclobutan]-4(3H)-one (500 mg, 1.87 mmol) and 1H-benzotriazole-1-methanol (586 mg, 3.93 mmol) in THF (5 mL) over 10 minutes in a dry ice-acetone bath under an argon atmosphere. The mixture was stirred for 0.5 hours in an ice bath, and then diluted with EtOAc (10 mL). After stirring for 0.5 hours, the mixture was filtered off. The filtrate was washed with 0.2 M aqueous NaOH (two times), water and brine, dried over MgSO4 and silicagel, filtered off. The filtrate was evaporated to give crude 6-bromo-3,3-bis(hydroxymethyl)spiro[chromene-2,1′-cyclobutan]-4(3H)-one (641 mg).

後処理

  1. stirringAfter stirring for 0.5 hours
  2. filtrationthe mixture was filtered off
  3. washThe filtrate was washed with 0.2 M aqueous NaOH (two times), water and brine
  4. dry with materialdried over MgSO4 and silicagel
  5. filtrationfiltered off
  6. customThe filtrate was evaporated

出典と根拠

ORDレコード
ord-8e4f8db5bb04459aa9692166d9fb027c
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242973B2

反応ノート

読み込み中…

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