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1H-Benzotriazole-1-methanol → HCID 86724237, 화합물

HRID 594845
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HRID 594845 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 2241691H-Benzotriazole-1-methanolHCID 23665647Potassium tert-butoxideHCID 667462536-Bromospiro[chroman-2,1'-cyclobutan]-4-one

생성물 1

HCID 86724237HCID 86724237, 화합물수율 104.8%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 8857
Ethyl Acetate
용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-8e4f8db5bb04459aa9692166d9fb027c
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242973B2

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