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Hydrochloric Acid → 3-(4-Fluoro-3-methoxyphenyl)prop-2-enoic acid

HRID 2100722
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인쇄 미리보기

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HRID 2100722 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[O:10][CH3:11].C(O)(=O)[CH2:13][C:14]([OH:16])=[O:15].Cl>N1C=CC=CC=1.N1CCCCC1>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH:13][C:14]([OH:16])=[O:15])=[CH:4][C:3]=1[O:10][CH3:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 867Malonic AcidHCID 27373584-Fluoro-3-methoxybenzaldehyde

생성물 1

HCID 534043133-(4-Fluoro-3-methoxyphenyl)prop-2-enoic acid수율 97%

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 8082Piperidine용매

반응 조건

온도
120 °C

실험 절차

A mixture of 4-Fluoro-3-methoxy-benzaldehyde (6.16 g, 40 mmol), and malonic acid (6.24 g, 60 mmol) in pyridine (30 ml) and piperidine (1 ml) was heated at 120° C. for 2 hrs. The mixture was cooled to room temperature and neutralized with concentrated HCl to PH<3, the white solid was collected and dried to give 7.6 g of product (97% yield). LC-MS: m/e 195 (M−1)

후처리

  1. customthe white solid was collected
  2. customdried

출처 및 근거

ORD 기록
ord-7c2cf292a17f448dae2c111e5cf6b23e
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572809B2

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