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Sodium hydride → 7-(6-hydroxycyclohex-2-enyl)hept-5Z-enoic acid

HRID 26310
ノート
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反応式

HRID 26310 の反応式
[H-].[Na+].[H][H].[Br-].[C:6]([CH2:9][CH2:10][CH2:11][CH2:12][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([OH:8])=[O:7].[CH:32]12[CH2:40][CH:39](O)[O:38][CH:37]1[CH2:36][CH2:35][CH:34]=[CH:33]2>CS(C)=O.O>[OH:38][CH:37]1[CH:32]([CH2:40]/[CH:39]=[CH:12]\[CH2:11][CH2:10][CH2:9][C:6]([OH:8])=[O:7])[CH:33]=[CH:34][CH2:35][CH2:36]1
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 24758Sodium hydrideHCID 161236(4-Carboxybutyl)triphenylphosphonium bromideHCID 203366972,3,3a,6,7,7a-Hexahydro-1-benzofuran-2-olHCID 178418361HCID 178418361、化合物

生成物 1

HCID 705963197-(6-hydroxycyclohex-2-enyl)hept-5Z-enoic acid収率 60.9%

試薬・触媒・溶媒 2

HCID 679
Dimethyl Sulfoxide
溶媒
2 回
HCID 962Water溶媒

実験手順

A 12.5 g (296 mmol) portion of sodium hydride (57% oil dispersion) was heated with 95 ml of dry dimethylsulfoxide (DMSO) under argon at 65°-75° for ca. 2.5 hr until hydrogen evolution had ceased. The mixture was stirred with ice-water cooling as 48.3 g (109 mmol) of 4-carboxybutyltriphenylphosphonium bromide (Aldrich) was added as a solid. The resultant deep red mixture was stirred at 0° for several minutes, then at room temperature until most of the salts had dissolved (1 hr). A solution of 12.2 g (87.1 mmol) of 7-oxabicyclo[4.3.0]non-2-en-8-ol in 10 ml of dry DMSO was added dropwise over 2 hr to the vigorously stirred ylide solution. The resultant dark mixture was stirred for 20 hr at room temperature. Water (200 ml) was added then and the resultant mixture was extracted three times with ethyl acetate and these extracts were discarded. The remaining aqueous phase was acidified with concentrated hydrochloric acid and then extracted four times with ethyl acetate. The combined extracts were dried (MgSO4) and evaporated in vacuo. The resultant residue was evaporated at 0.1 mm as the pot was warmed to 50° and the receiver flask was cooled in an acetone-dry bath. The yield of crude orange oil was 32.5 g (theoretical yield 19.5 g) and contained in addition to the desired product, considerable aromatic byproduct as evidenced from an nmr spectrum of this oil. This oil was extracted several times with warm ether-pentane (1:1). The combined extracts were dried (MgSO4) and evaporated in vacuo to give 11.9 g of 7-(6-hydroxycyclohex-2-enyl)hept-5Z-enoic acid. A portion of this product was purified by column chromatography on silicic acid-Celite (85:15) using benzene to ethyl acetate gradient elution to obtain pure 7-(6-hydroxycyclohex-2-enyl)hept-5Z-enoic acid.

後処理

  1. additionwas added as a solid
  2. dissolutionat room temperature until most of the salts had dissolved (1 hr)
  3. stirringThe resultant dark mixture was stirred for 20 hr at room temperature
  4. extractionthe resultant mixture was extracted three times with ethyl acetate
  5. extractionextracted four times with ethyl acetate
  6. dry with materialThe combined extracts were dried (MgSO4)
  7. customevaporated in vacuo
  8. customThe resultant residue was evaporated at 0.1 mm as the
  9. temperaturepot was warmed to 50°
  10. temperaturethe receiver flask was cooled in an acetone-
  11. customdry bath
  12. additioncontained in addition to the desired product, considerable aromatic byproduct
  13. extractionThis oil was extracted several times with warm ether-pentane (1:1)
  14. dry with materialThe combined extracts were dried (MgSO4)
  15. customevaporated in vacuo

出典と根拠

ORDレコード
ord-d56a26a5e6b744b08f0c476045507f10
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04149017

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