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Acetic Acid → 6-(2-Tetrahydropyranyloxy)hexanal

HRID 1581107
ノート
印刷プレビュー

反応式

HRID 1581107 の反応式
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][OH:14].C(N(CC)CC)C.C(O)(=O)C.O>CS(C)=O.C(OCC)C>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]=[O:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 176Acetic AcidHCID 962WaterHCID 8471TriethylamineHCID 5589936-(Tetrahydro-2H-pyran-2-yloxy)-1-hexanol

生成物 1

HCID 108673416-(2-Tetrahydropyranyloxy)hexanal収率 64.5%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒2 回
HCID 3283
Diethyl Ether
溶媒

実験手順

Pyridine-sulphur trioxide complex (17.1 g., 0.108 mole) in dimethylsulphoxide (90 ml.) was added dropwise to a mixture of 6-(2-tetrahydropyranyloxy)-hexanol (7.2 g., 0.036 mole) and triethylamine (27 g., 0.27 mole) in dimethylsulphoxide (90 ml.) at 25°C. The mixture was stirred for a further hour, then 2N acetic acid (100 ml.), water (200 ml.) and diethyl ether (500 ml.) added successively, the layers separated and the aqueous layer extracted with diethyl ether. The combined ether solutions were washed quickly with 2N hydrochloric acid, aqueous sodium carbonate and then water, and dried over sodium sulphate. The solvent was evaporated and the residue distilled under reduced pressure to give 6-(2-tetrahydropyranyloxy)hexanal (4.65 g., 63%), b.p. 75°-105°C./0.15 mm.Hg.

後処理

  1. customthe layers separated
  2. extractionthe aqueous layer extracted with diethyl ether
  3. washThe combined ether solutions were washed quickly with 2N hydrochloric acid, aqueous sodium carbonate
  4. dry with materialwater, and dried over sodium sulphate
  5. customThe solvent was evaporated
  6. distillationthe residue distilled under reduced pressure

出典と根拠

ORDレコード
ord-7dcf48507b3b45e296cd447f1d07488f
出典データセット
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03935261

反応ノート

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