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Sulfuric Acid → 2-Hydroxytricyclo(3.3.1.13,7)decane-2-carbonitrile

HRID 745853
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반응식

HRID 745853 반응식
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[C:2]1=[O:11])[CH2:8]2.S(=O)(=O)(O)O.[C-:17]#[N:18].[Na+].CCOCC>CO>[C:17]([C:2]1([OH:11])[CH:3]2[CH2:9][CH:7]3[CH2:6][CH:5]([CH2:10][CH:1]1[CH2:8]3)[CH2:4]2)#[N:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 3283Diethyl EtherHCID 8929Sodium CyanideHCID 64151Adamantanone

생성물 1

HCID 34511512-Hydroxytricyclo(3.3.1.13,7)decane-2-carbonitrile수율 81%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a well stirred solution of 2-adamantanone (45.0 grams, 0.3 mol) in 200 ml methanol were added 50 ml concentrated sulfuric acid at a rate that caused the solution to reflux. Then a saturated aqueous solution of sodium cyanide (88.2 grams, 0.6 mol) was added, and the mixture was first refluxed for 1 hour and then stirred at room temperature for 3 additional hours. Ether was added, and the organic solution was decanted from the precipitated salts. The ether solution was washed with an aqueous solution of sodium chloride and water and then dried and evaporated to leave 43.0 grams (81%) of compound 4 as a beige crystalline solid, melting point >240° C. (decomposition).

후처리

  1. temperatureto reflux
  2. temperaturethe mixture was first refluxed for 1 hour
  3. customthe organic solution was decanted from the precipitated salts
  4. washThe ether solution was washed with an aqueous solution of sodium chloride and water
  5. customdried
  6. customevaporated

출처 및 근거

ORD 기록
ord-6f3e91c38f514c1bb5876fbd2ae751b8
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04600782

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