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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 4-(trans-4-Decenyloxy)-benzoic acid

HRID 369539
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인쇄 미리보기

반응식

HRID 369539 반응식
C[O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13]/[CH:14]=[CH:15]/[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:6][CH:5]=1.O.O.[OH-].[Li+].Cl>CO>[CH2:11]([O:10][C:7]1[CH:6]=[CH:5][C:4]([C:3]([OH:21])=[O:2])=[CH:9][CH:8]=1)[CH2:12][CH2:13]/[CH:14]=[CH:15]/[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962Water2회HCID 168937Lithium hydroxide, monohydrateHCID 18521044Methyl-4-(trans-4-decenyloxy)-benzoate

생성물 1

HCID 185210594-(trans-4-Decenyloxy)-benzoic acid수율 85.1%

시약·촉매·용매 1

HCID 887Methanol
용매

실험 절차

The ester 35i (500 mg, 1.7 mmol) was dissolved in 50 ml methanol. Water (approximately 10 ml) was added until the solution remained cloudy, at which time lithium hydroxide monohydrate (723 mg, 17.0 mmol) was added. The reaction mixture was refluxed overnight and acidified with concentrated HCl. Water was added (approximately 30 ml), the mixture was cooled, filtered, washed with water and allowed to air dry yielding 400 mg (84%) of a white powder.

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was refluxed overnight
  3. temperaturethe mixture was cooled
  4. filtrationfiltered
  5. washwashed with water
  6. customto air dry

출처 및 근거

ORD 기록
ord-da62695761de4d9db9c706e6c545204f
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06139771

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