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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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6-(Benzyloxy)benzo[c][1,2]oxaborol-1(3H)-ol → 1,3-Dihydro-2,1-benzoxaborole-1,6-diol

HRID 529194
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인쇄 미리보기

반응식

HRID 529194 반응식
C([O:8][C:9]1[CH:18]=[CH:17][C:12]2[CH2:13][O:14][B:15]([OH:16])[C:11]=2[CH:10]=1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[OH:8][C:9]1[CH:18]=[CH:17][C:12]2[CH2:13][O:14][B:15]([OH:16])[C:11]=2[CH:10]=1
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참가 물질

5

반응물 2

HCID 529192896-(Benzyloxy)benzo[c][1,2]oxaborol-1(3H)-olHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 529192911,3-Dihydro-2,1-benzoxaborole-1,6-diol수율 98%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

H178 (13 mmol) was dissolved in MeOH (300 mL). To this solution under nitrogen was added 10% Pd/C (200 mg). The reaction mixture was vacuumed and backfilled hydrogen for 3 times, then stirred overnight at room temperature. After filtration and rotary evaporation, the residue was purified by recrystallization to give H181 (1.98 mg, 98% yield). 1H NMR (300 MHz, DMSO-d6): δ 9.29 (s, 1H), 9.04 (s, 1H), 7.18 (d, J=8.4 Hz, 2H), 6.87 (dd, J=8.1 & 2.4 Hz, 1H) and 4.86 (s, 2H) ppm. Mp 133-135° C.

후처리

  1. filtrationAfter filtration and rotary evaporation
  2. customthe residue was purified by recrystallization
  3. customto give H181 (1.98 mg, 98% yield)

출처 및 근거

ORD 기록
ord-27468fa9debe4e5fb1b943adac655803
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346834B2

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