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HCID 12782916, 화합물 → HCID 12731441, 화합물

HRID 2049141
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HRID 2049141 반응식
O[CH2:2][CH:3]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[C:4]([OH:6])=[O:5]>P(=O)(O)(O)O>[CH2:7]([C:3](=[CH2:2])[C:4]([OH:6])=[O:5])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 12782916HCID 12782916, 화합물

생성물 1

HCID 12731441HCID 12731441, 화합물수율 77%

시약·촉매·용매 1

HCID 1004Phosphoric Acid촉매

실험 절차

A 34.25 g sample of α-hydroxymethylpalmitic acid (0.119 mole) and 17 drops of phosphoric acid (85%) were placed in a distillation flask and the mixture heated to 245°-255° C. in an oil bath under vacuum. The product, 2-tetradecylacrylic acid, distilled over at 155°-160° C. at 0.10 mm Hg (24.80 g; 77% yield) and was crystallized from acetone, m.p. 53°-55° C.

후처리

  1. temperaturethe mixture heated to 245°-255° C. in an oil bath under vacuum
  2. distillationThe product, 2-tetradecylacrylic acid, distilled over at 155°-160° C. at 0.10 mm Hg (24.80 g; 77% yield)
  3. customwas crystallized from acetone, m.p. 53°-55° C.

출처 및 근거

ORD 기록
ord-abc4bd6d267645b3b9e4ab52cf8c9738
출처 데이터셋
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04196300

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