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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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11-Phenoxyundecanoic acid → 11-Phenoxy-1-undecanol

HRID 2051905
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인쇄 미리보기

반응식

HRID 2051905 반응식
B#B.[O:3]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20](O)=[O:21])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O1CCCC1>[O:3]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][OH:21])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8159711-Phenoxyundecanoic acidHCID 6328200Diboron

생성물 1

HCID 1157250211-Phenoxy-1-undecanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To 100 ml of 1M diborane in tetrahydrofuran under nitrogen chilled in an ice bath is added dropwise 13.92 g of 11-phenoxyundecanoic acid in 50 ml of tetrahydrofuran over 30 minutes. The solution is allowed to stand at room temperature for 19 hours and is poured onto ice. After standing, the mixture is filtered and the solid washed with water to give white crystals, mp 56°-58° C. A sample on recrystallization from ethanol gives white crystals, mp 56.5°-57.5° C.

후처리

  1. additionis poured onto ice
  2. filtrationthe mixture is filtered
  3. washthe solid washed with water
  4. customto give white crystals, mp 56°-58° C
  5. customA sample on recrystallization from ethanol
  6. customgives white crystals, mp 56.5°-57.5° C.

출처 및 근거

ORD 기록
ord-398688844dd443709b9e67856e538ff6
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04182776

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