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Boron tribromide → HCID 23050232, 화합물

HRID 978732
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HRID 978732 반응식
C[O:2][C:3]1[C:13]([O:14]C)=[CH:12][C:6]2[S:7][C:8]([C:10]#[N:11])=[CH:9][C:5]=2[CH:4]=1.B(Br)(Br)Br>ClCCl>[OH:2][C:3]1[C:13]([OH:14])=[CH:12][C:6]2[S:7][C:8]([C:10]#[N:11])=[CH:9][C:5]=2[CH:4]=1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 23050245HCID 23050245, 화합물

생성물 1

HCID 23050232HCID 23050232, 화합물수율 95.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
-70 °C

실험 절차

5,6-Dimethoxy-benzo[b]thiophene-2-carbonitrile (9.0 g) was dissolved in dichloromethane (135 ml) and the solution was stirred and cooled to -70° C. and treated at a rapid dropwise rate with a cold solution of boron tribromide (19.5 ml) in dichloromethane (60 ml). The resultant suspension was stirred at room temperature for 1 h. then poured into ice-cold water (1000 ml). The light coloured solid was filtered, dried, dissolved in acetone:hexane (1:1) then eluted through coarse silica (0.2-0.5 mm, Merck, 50 g) in acetone:hexane (1:1). The appropriate fractions were combined, evaporated to dryness and crystallised from acetone/n-hexane to give 5,6-dihydroxy-benzo[b]thiophene-2-carbonitrile (7.5 g), m.p. 229°-230° C.

후처리

  1. filtrationwas filtered
  2. customdried
  3. dissolutiondissolved in acetone:hexane (1:1)
  4. washthen eluted through coarse silica (0.2-0.5 mm, Merck, 50 g) in acetone:hexane (1:1)
  5. customevaporated to dryness
  6. customcrystallised from acetone/n-hexane

출처 및 근거

ORD 기록
ord-e47f5280f2e94879b576bf2336dbc6c1
출처 데이터셋
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04665206

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