(Z)-(3-nonenyl)-triphenylphosphonium iodide → (Z,Z)-2-[(2,2-dimethyl-3,6-dodecadienyl)oxy]-tetrahydro-2H-pyran

HRID 1388644

反応式

HRID 1388644 の反応式
C([Li])CCC.[I-].[CH2:7]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[CH3:35][C:36]([CH3:47])([CH2:39][O:40][CH:41]1[CH2:46][CH2:45][CH2:44][CH2:43][O:42]1)[CH:37]=O>O1CCCC1.CN(C)P(=O)(N(C)C)N(C)C.O1CCCC1.[Cl-].[Na+].O>[CH3:35][C:36]([CH3:47])(/[CH:37]=[CH:7]\[CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH2:39][O:40][CH:41]1[CH2:46][CH2:45][CH2:44][CH2:43][O:42]1

参加物

7

反応物 3

HCID 10984097(Z)-(3-nonenyl)-triphenylphosphonium iodideHCID 132764582,2-Dimethyl-3-((tetrahydro-2H-pyran-2-yl)oxy)propanalHCID 178418339Butyllithium

生成物 1

HCID 70507643(Z,Z)-2-[(2,2-dimethyl-3,6-dodecadienyl)oxy]-tetrahydro-2H-pyran収率 90.3%

試薬・触媒・溶媒 3

HCID 8028Tetrahydrofuran溶媒HCID 57417360Sodium chloride; water溶媒HCID 86583969tetrahydrofuran HMPA溶媒

反応条件

温度
-78 °C

実験手順

A 2.7 ml portion of n-butyllithium (1.6 M in hexane) was slowly added at -76° C., under argon to a solution of 2.7 g (5.24 mmoles) of (Z)-(3-nonenyl)-triphenylphosphonium iodide in a mixture of 7.5 ml of 2:1 tetrahydrofuran-hexamethylphosphorictriamide by syringe. The solution turned orange-red in color. Without delay, a solution of 0.700 g (3.76 mmoles) of 2,2-dimethyl-3-[(tetrahydro-2H-pyran-2-yl)oxy]-propanal in 1 ml of tetrahydrofuran was added dropwise to the solution. The resulting mixture was stirred at -78° C. for 30 minutes. The temperature was then allowed to rise to 0° C. After 1 hour, the reaction mixture was poured into brine, and the product extracted twice with 1:1 hexane-ether. The organic layer was dried using MgSO4, and the solvents evaporated in vacuo. Purification of the crude product by rapid chromatography on a silica-gel column gave 1.0 g (90.2%) of (Z,Z)-2-[(2,2-dimethyl-3,6-dodecadienyl)oxy]-tetrahydro- 2H-pyran. This material was dissolved in 10 ml of methanol and treated with 0.1 ml of 2 N hydrochloric acid. After stirring for 2 hours at room temperature, the volume of methanol was reduced to about 3 ml by concentration under reduced pressure. The remaining solution was diluted with ether, and the ether solution washed with saturated sodium bicarbonate solution and brine and thereafter dried using MgSO4 and then concentrated under reduced pressure. The residue (0.780 g) was chromatographed on a silica gel column. Hexane-ether (4:1) eluted 0.690 g (79.1%) of pure (Z,Z)-2,2-dimethyl-3,6-dodecadien-1-ol. (98.6% pure by GC-analysis).

後処理

  1. customto rise to 0° C
  2. waitAfter 1 hour
  3. extractionthe product extracted twice with 1:1 hexane-ether
  4. customThe organic layer was dried
  5. customthe solvents evaporated in vacuo
  6. customPurification of the crude product by rapid chromatography on a silica-gel column

出典と根拠

ORDレコード
ord-23097451c6d84735853c98f3f2e3af5c
出典データセット
uspto-grants-1984_02
特許番号
US04432906

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