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2-methylspiro[3.3]heptane-2-carboxylic acid → HCID 20320778, 화합물

HRID 866395
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HRID 866395 반응식
[CH3:1][C:2]1([C:9]([OH:11])=O)[CH2:5][C:4]2([CH2:8][CH2:7][CH2:6]2)[CH2:3]1.[CH3:12][Li]>CCOCC>[CH3:1][C:2]1([C:9](=[O:11])[CH3:12])[CH2:3][C:4]2([CH2:6][CH2:7][CH2:8]2)[CH2:5]1
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참가 물질

4

반응물 2

HCID 203207772-methylspiro[3.3]heptane-2-carboxylic acidHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 20320778HCID 20320778, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

반응 조건

온도
25 °C

실험 절차

A solution of 5.0 g (33.0 mmol) 2-methylspiro[3.3]heptane-2-carboxylic acid in 33.0 ml of dry ether was stirred under argon at 0° C and 47.6 ml (74.3 mmol) of 1.56 M methyl lithium in ether added dropwise. The reaction mixture was allowed to warm to 25° C and was stirred for 3.0 hr. The reaction mixture was cooled to -20° C and quenched by addition of 10% aqueous HCl. The layers were separated and the aqueous layer extracted with ether. The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine, then dried (MgSO4), filtered, and evaporated in vacuo to afford 2-methyl-2-acetylspiro[3.3]heptane as a light yellow oil (4.91 g 98%).

후처리

  1. temperatureThe reaction mixture was cooled to -20° C
  2. customquenched by addition of 10% aqueous HCl
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with ether
  5. washThe combined organic layers were washed with saturated aqueous sodium bicarbonate and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-50122c90e0b540f0acefcad7db2d1dc0
출처 데이터셋
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04098823

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