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Hydrochloric Acid → HCID 21546969、化合物

HRID 1605491
ノート
印刷プレビュー

反応式

HRID 1605491 の反応式
[OH:1][C:2]1([C:7]#N)[CH2:6][CH:5]=[CH:4][CH2:3]1.C[OH:10].Cl.C([O:14][CH2:15]C)C>>[OH:1][C:2]1([C:7]([O:14][CH3:15])=[O:10])[CH2:6][CH:5]=[CH:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 3283Diethyl EtherHCID 21546968HCID 21546968、化合物

生成物 1

HCID 21546969HCID 21546969、化合物

実験手順

A solution of 150 mg. of 1-hydroxy-3-cyclopentene-1-carbonitrile in 10 ml. of anhydrous methanol and 5 ml. of anhydrous diethyl ether is cooled in an ice-bath. The solution is saturated with gaseous hydrogen chloride, then allowed to warm to room temperature and finally set aside overnight. The solution is then concentrated in vacuo to a solid, which is dissolved in approximately 10 ml. of water. After 23/4 hours an aliquot is removed and extracted with methylene chloride. The extract is dried using sodium sulfate, and it is concentrated in vacuo giving methyl 1-hydroxy-3-cyclopentene-1-carboxylate as a yellowish oil. The infrared spectrum of the product (in CDCl3) shows an absorption at 1730 cm-1, confirming the presence of an ester function. The nmr spectrum of the product (in CDCl3) shows absorptions at 5.7 ppm (singlet, olefinic hydrogens), 3.8 ppm (singlet, methyl hydrogens) and 3.3-2.2 ppm (singlet superimposed on a quartet, hydroxy group and methylene hydrogens). The remainder of the aqueous solution is worked up analogously to give a further quantity of product. The combined yield is 65.8 mg.

後処理

  1. concentrationThe solution is then concentrated in vacuo to a solid, which
  2. dissolutionis dissolved in approximately 10 ml
  3. customAfter 23/4 hours an aliquot is removed
  4. extractionextracted with methylene chloride
  5. customThe extract is dried
  6. concentrationis concentrated in vacuo

出典と根拠

ORDレコード
ord-0c9aaafc3e6042b298c3e8bd63d556cb
出典データセット
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03950390

反応ノート

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