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

HRID 745853
ノート
印刷プレビュー

反応式

HRID 745853 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-6f3e91c38f514c1bb5876fbd2ae751b8
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04600782

反応ノート

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