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2,3-Dihydroxybutanedioic Acid → HCID 86756217, 화합물

HRID 565741
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HRID 565741 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][CH:7]=1.[C:16]([OH:25])(=[O:24])[CH:17]([CH:19]([C:21]([OH:23])=[O:22])[OH:20])[OH:18]>O>[C:21]([CH:19]([CH:17]([C:16]([OH:25])=[O:24])[OH:18])[OH:20])([OH:23])=[O:22].[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8752,3-Dihydroxybutanedioic AcidHCID 11506782N-(3-Chlorophenyl)benzenemethanamine

생성물 1

HCID 86756217HCID 86756217, 화합물수율 29.3%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

(3-Chlorophenyl)phenylmethylamine (9.25g, 42.5 mmol) and (−)-tartaric acid (7.02 g, 46.7 mmol) were dissolved in water (40 ml) with heating. Thereafter, the precipitated crude crystals obtained by allowing to cool the reaction solution to room temperature were collected by filtration. The resulting crystals were purified by repeatedly recrystallizing from water, to give (−)-(3-chlorophenyl)phenylmethylamine (−)-tartrate (4.58 g).

후처리

  1. temperaturewith heating
  2. customThereafter, the precipitated crude crystals
  3. customobtained
  4. filtrationwere collected by filtration
  5. customThe resulting crystals were purified
  6. customby repeatedly recrystallizing from water

출처 및 근거

ORD 기록
ord-ae3045ec0c1c4399aa342bbe87b7f42d
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06172228B2

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