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Water → 1,2-Propanediol, 3-((p-benzyloxy)phenoxy)-

HRID 330498
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인쇄 미리보기

반응식

HRID 330498 반응식
CC1(C)[O:6][CH:5]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11][CH:10]=2)[CH2:4][O:3]1.O>C(Cl)Cl>[C:17]1([CH2:16][O:15][C:12]2[CH:13]=[CH:14][C:9]([O:8][CH2:7][CH:5]([OH:6])[CH2:4][OH:3])=[CH:10][CH:11]=2)[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 133384952,2-Dimethyl-4-[[4-(phenylmethoxy)phenoxy]methyl]-1,3-dioxolane

생성물 1

HCID 2310801,2-Propanediol, 3-((p-benzyloxy)phenoxy)-수율 38.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 8.98 g of 2,2-dimethyl-4-[[4-(phenylmethoxy)phenoxy]methyl]-1,3-dioxolane, 15 g of a strongly acidic ion exchange resin and 200 ml of water was refluxed for 24 hours, then allowed to cool and methylene chloride was added. The mixture was filtered and the organic layer separated and saved. The aqueous layer was extracted several times with methylene chloride. All organic solutions were combined, dried and evaporated, giving 3.0 g of the desired compound, mp 125°-127° C.

후처리

  1. temperaturewas refluxed for 24 hours
  2. temperatureto cool
  3. filtrationThe mixture was filtered
  4. customthe organic layer separated
  5. extractionThe aqueous layer was extracted several times with methylene chloride
  6. customdried
  7. customevaporated

출처 및 근거

ORD 기록
ord-2a0a8a14e4764440bb210a90b3124989
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04897385

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