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Thioglycolic Acid → (4,5-Dihydroxy-10-oxo-9,10-dihydro-anthracen-9-ylsulfanyl)-acetic acid

HRID 1651144
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반응식

HRID 1651144 반응식
Br[CH:2]1[C:15]2[C:10](=[C:11]([OH:16])[CH:12]=[CH:13][CH:14]=2)[C:9](=[O:17])[C:8]2[C:7]([OH:18])=[CH:6][CH:5]=[CH:4][C:3]1=2.[SH:19][CH2:20][C:21]([OH:23])=[O:22]>ClCCl>[C:21]([CH2:20][S:19][CH:2]1[C:15]2[C:10](=[C:11]([OH:16])[CH:12]=[CH:13][CH:14]=2)[C:9](=[O:17])[C:8]2[C:7]([OH:18])=[CH:6][CH:5]=[CH:4][C:3]1=2)([OH:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1133Thioglycolic AcidHCID 27650410-Bromo-1,8-dihydroxy-10H-anthracen-9-one

생성물 1

HCID 20067256(4,5-Dihydroxy-10-oxo-9,10-dihydro-anthracen-9-ylsulfanyl)-acetic acid수율 75%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

10-Bromo-1,8-dihydroxy-9-anthrone (305 mg) was dissolved in dichloromethane (10 ml) and mercaptoacetic acid (0.07 ml) was added. The solution was stirred at room temperature for 3 days, during which time a yellow precipitate was formed, which was filtered off and recrystallised from absolute ethanol to give 10-(carboxymethylthio)-1,8-dihydroxy-9-anthrone (237 mg, 75%) as yellow needles, melting point 151°-152° C. (Found: C 60.9, H 3.8, S 10.1%; M=316.0410; C16H12O5S requires C 60.75, H3.8, S 10.1%, M=316.0405).

후처리

  1. customwas formed
  2. filtrationwhich was filtered off
  3. customrecrystallised from absolute ethanol

출처 및 근거

ORD 기록
ord-cadb5125807f4fd4a30b61751d33355e
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04927845

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