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Sodium borohydride → 4,5 Dihydroxymethyl-2,2': 5',2"-terthiophene

HRID 1599514
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HRID 1599514 반응식
[CH:1]([C:3]1[CH:4]=[C:5]([C:10]2[S:11][C:12]([C:15]3[S:16][CH:17]=[CH:18][CH:19]=3)=[CH:13][CH:14]=2)[S:6][C:7]=1[CH2:8][OH:9])=[O:2].[BH4-].[Na+]>CO>[OH:2][CH2:1][C:3]1[CH:4]=[C:5]([C:10]2[S:11][C:12]([C:15]3[S:16][CH:17]=[CH:18][CH:19]=3)=[CH:13][CH:14]=2)[S:6][C:7]=1[CH2:8][OH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 573213644-Formyl-5-hydroxymethyl-2,2':5', 2"-terthiophene

생성물 1

HCID 539277724,5 Dihydroxymethyl-2,2': 5',2"-terthiophene수율 99.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 4-formyl-5-hydroxymethyl-2,2':5', 2"-terthiophene (0.1 g) in methanol (10 ml) was added excess amount of sodium borohydride. The reaction mixture was stirred at room temperature for 40 minutes. Methanol was removed and water was added. The solution was extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate and concentrated to give brownish solid product (0.1 g), melting point 99°-101° C.

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후처리

  1. customMethanol was removed
  2. additionwater was added
  3. extractionThe solution was extracted with ethyl acetate
  4. washwashed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f19eeda0b721487885aad9595c2afa01
출처 데이터셋
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05741811

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