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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(3-Chloropropyl)-2-methyl-1,3-dioxolane → 2-(3-Bromopropyl)-2-methyl-1,3-dioxolane

HRID 1106288
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반응식

HRID 1106288 반응식
[CH2:1]1[O:10][C:4]([CH2:6][CH2:7][CH2:8]Cl)([CH3:5])[O:3][CH2:2]1.[Br-:11].[Li+].C(N(C(C)C)CC)(C)C>O1CCCC1>[CH2:1]1[O:10][C:4]([CH2:6][CH2:7][CH2:8][Br:11])([CH3:5])[O:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 800792-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 81531DiisopropylethylamineHCID 82050Lithium Bromide

생성물 1

HCID 5600542-(3-Bromopropyl)-2-methyl-1,3-dioxolane

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

4.0 grams of 5-chloro-2-pentanone ethylene ketal is mixed with 9.0 grams of lithium bromide and 2.0 grams of diisopropylethylamine in 30 ml of tetrahydrofuran which has been distilled from lithium aluminum hydride. The mixture is refluxed under nitrogen for 48 hours, cooled and poured into a mixture of ether and water for extraction. The ether layer is washed twice with water, then with 1 N hydrochloric acid and then twice again with water. The ether layer is then dried over sodium sulfate and evaporated under reduced pressure to give title product.

후처리

  1. distillationhas been distilled from lithium aluminum hydride
  2. temperatureThe mixture is refluxed under nitrogen for 48 hours
  3. temperaturecooled
  4. additionpoured into a mixture of ether and water for extraction
  5. washThe ether layer is washed twice with water
  6. dry with materialThe ether layer is then dried over sodium sulfate
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-045cd49e555340efa01e591f3b47857e
출처 데이터셋
uspto-grants-1982_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04312994

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