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Glycolic Acid → 2-(4-Chloro-2-methylphenoxymethyl)-1,3-dioxolan-4-one

HRID 372339
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HRID 372339 반응식
[C:1]([OH:5])(=[O:4])[CH2:2]O.[Cl:6][C:7]1[CH:16]=[CH:15][C:10]([O:11][CH2:12][CH:13]=[O:14])=[C:9]([CH3:17])[CH:8]=1.B(F)(F)F.CCOCC>CCOCC.O1CCCC1>[Cl:6][C:7]1[CH:16]=[CH:15][C:10]([O:11][CH2:12][CH:13]2[O:5][C:1](=[O:4])[CH2:2][O:14]2)=[C:9]([CH3:17])[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 757Glycolic AcidHCID 8000Boron trifluoride etherateHCID 123914592-(4-Chloro-2-methylphenoxy)acetaldehyde

생성물 1

HCID 203271852-(4-Chloro-2-methylphenoxymethyl)-1,3-dioxolan-4-one수율 62.6%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran
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용매

실험 절차

A solution containing 2.5g (0.033 mole) of glycolic acid, 4.2g (0.025 mole) of 4-chloro-2-methylphenoxyacetaldehyde and 10g (0.07 mole) of boron trifluoride etherate in 50 ml of ether and 30 ml of tetrahydrofuran was allowed to stand at room temperature for 24 hours. The dark solution was washed with aqueous sodium bicarbonate, dried and concentrated to dryness. Recrystallization from ether-hexane gave 3.8g of 2-(4-chloro-2-methylphenoxymethyl)-1,3-dioxolan-4-one having a melting point of 42°-44°.

후처리

  1. washThe dark solution was washed with aqueous sodium bicarbonate
  2. customdried
  3. concentrationconcentrated to dryness
  4. customRecrystallization from ether-hexane

출처 및 근거

ORD 기록
ord-970614a4618c4c47a14462efc5ea1cc7
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04090861

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