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Hydrochloric Acid → 4-Pentyl-3-cyclohexen-1-methanol

HRID 326958
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HRID 326958 반응식
[CH2:1]([C:6]1[CH2:11][CH2:10][CH:9]([C:12](O)=[O:13])[CH2:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[Li].[H-].Cl>O1CCCC1.O>[CH2:1]([C:6]1[CH2:11][CH2:10][CH:9]([CH2:12][OH:13])[CH2:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 166653HydrideHCID 3028194LithiumHCID 140668384-Pentyl-3-cyclohexenylcarboxylic acid

생성물 1

HCID 197340354-Pentyl-3-cyclohexen-1-methanol

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
3회

실험 절차

A solution of 4-pentyl-3-cyclohexen-l-carboxylic acid (3.4 g) in tetrahydrofurn (THF; 55 ml) was added dropwise to a cold (0° C.) solution of lithium aluminim hydride (1.37 g) in tetrahydrofuran (THF, 55 ml), in a flask equipped with a condenser. The reaction mixture was stirred at room temperature for at least three hours, re-cooled to 0° C., and water (8 ml) was then added dropwise. An additional 55 ml of THF was added, and the reaction mixture stirred for three hours. The reaction mixture was then acidified with 2 M HCl (150 ml), and extracted with a 1:1 (v:v) ethyl acetate:hexane mixture. The combined organic layers were extracted with saturated sodium chloride and dried over sodium sulfate. The solvent was removed in vacuo, and the resultant oil was distilled (92°-95° C. at c.a. 1 mm Hg) to produce 4-pentyl-3-cyclohexen-1-methanol.

후처리

  1. customequipped with a condenser
  2. temperaturere-cooled to 0° C.
  3. stirringthe reaction mixture stirred for three hours
  4. extractionextracted with a 1:1 (v:v) ethyl acetate
  5. extractionThe combined organic layers were extracted with saturated sodium chloride
  6. dry with materialdried over sodium sulfate
  7. customThe solvent was removed in vacuo
  8. distillationthe resultant oil was distilled (92°-95° C. at c.a. 1 mm Hg)

출처 및 근거

ORD 기록
ord-022544d684034edfb1e62bc9026382bc
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05271864

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