Pyridine → Cyclooctyl methyl carbonate

HRID 258586

反応式

HRID 258586 の反応式
Cl[C:2]([O:4][CH3:5])=[O:3].[CH:6]1([OH:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.N1C=CC=CC=1.Cl.N1C=CC=CC=1>C1C=CC=CC=1>[C:2](=[O:3])([O:14][CH:6]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)[O:4][CH3:5]

参加物

6

反応物 4

HCID 1049PyridineHCID 6586Methyl chloroformate2 回HCID 12766CyclooctanolHCID 10176127Pyridinium chloride

生成物 1

HCID 109116Cyclooctyl methyl carbonate

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

18.9 gm of methyl chloroformate were added drop-by-drop under agitation to a solution of 25.6 gm of cyclooctanol and 15.8 gm of absolute pyridine in 150 ml of dry benzene under external cooling at 0° to 5° C. After the methyl chloroformate had been added, agitation was continued for 12 hours at room temperature. Then, the benzene phase was drawn off from the precipitated pyridine hydrochloride, and washed with diluted hydrochloric acid, sodium hydroxide solution and water, and dried. After the solvent had been distilled off, the raw ester was distilled in vacuo by means of a Vigreux column. A colorless liquid was obtained which had a herbal, very natural and complex fragrance which is distinguished by a strong and long-clinging flowery jasmine scent.

後処理

  1. temperatureunder external cooling at 0° to 5° C
  2. washwashed with diluted hydrochloric acid, sodium hydroxide solution and water
  3. customdried
  4. distillationAfter the solvent had been distilled off
  5. distillationthe raw ester was distilled in vacuo by means of a Vigreux column
  6. customA colorless liquid was obtained which

出典と根拠

ORDレコード
ord-71b68d19900b4363a424a4aa96159639
出典データセット
uspto-grants-1977_07
特許番号
US04033993

関連ノート

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