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Hydrochloric Acid → HCID 54253886, 화합물

HRID 724791
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HRID 724791 반응식
[OH-].[Na+].[Cl:3][C:4]1[CH:16]=[C:15]([Cl:17])[C:14]([O:18][CH3:19])=[CH:13][C:5]=1[O:6][C@@H:7]([CH3:12])[C:8]([O:10]C)=[O:9].Cl>C(O)C>[Cl:3][C:4]1[CH:16]=[C:15]([Cl:17])[C:14]([O:18][CH3:19])=[CH:13][C:5]=1[O:6][C@@H:7]([CH3:12])[C:8]([OH:10])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 54514488HCID 54514488, 화합물

생성물 1

HCID 54253886HCID 54253886, 화합물수율 97.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

125 ml (0.125 mol) of 1M sodium hydroxide solution were added to a solution of 34.9 g (0.125 mol) of methyl (S)-2-(2,4-dichloro-5-methoxyphenoxy)-propionate in 200 ml of ethanol. The solution was stirred at room temperature for 40 minutes and then adjusted to pH 1 with 2M hydrochloric acid. Most of the solvent was evaporated and the residue was partitioned between 400 ml of ethyl acetate and 400 ml of water. The separated organic phase was dried over anhydrous magnesium sulphate and evaporated to give 32.4 g (97.7%) of (S)-2-(2,4-dichloro-5-methoxyphenoxy)-propionic acid as a white solid, m.p. 114°-115° C.

후처리

  1. customMost of the solvent was evaporated
  2. customthe residue was partitioned between 400 ml of ethyl acetate and 400 ml of water
  3. dry with materialThe separated organic phase was dried over anhydrous magnesium sulphate
  4. customevaporated

출처 및 근거

ORD 기록
ord-24ef04ea611b407abb5ac29b1c292588
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05705492

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