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Sulfuric Acid → HCID 15295001、化合物

HRID 327944
ノート
印刷プレビュー

反応式

HRID 327944 の反応式
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:18]=[CH:17][C:11]2[C:12](=[O:16])[CH2:13][CH2:14][O:15][C:10]=2[C:9]=1[CH2:19][CH2:20][CH3:21].C([O:24][C:25]([C:27]1[O:28][C:29]2[C:35]([OH:36])=[CH:34][CH:33]=[CH:32][C:30]=2[CH:31]=1)=[O:26])C.C(=O)([O-])[O-].[K+].[K+].O.[OH-].[Li+].S(=O)(=O)(O)O>C1COCC1.O.C(OCC)(=O)C.CCOCC.CC(=O)CC>[O:16]=[C:12]1[C:11]2[CH:17]=[CH:18][C:8]([O:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][O:36][C:35]3[C:29]4[O:28][C:27]([C:25]([OH:26])=[O:24])=[CH:31][C:30]=4[CH:32]=[CH:33][CH:34]=3)=[C:9]([CH2:19][CH2:20][CH3:21])[C:10]=2[O:15][CH2:14][CH2:13]1
参加物実験手順後処理出典と根拠反応ノート

参加物

11

反応物 5

HCID 1118Sulfuric AcidHCID 11430Potassium CarbonateHCID 168937Lithium hydroxide, monohydrateHCID 19921918HCID 19921918、化合物HCID 21400703Ethyl 7-hydroxy-1-benzofuran-2-carboxylate

生成物 1

HCID 15295001HCID 15295001、化合物収率 74.9%

試薬・触媒・溶媒 5

HCID 962Water溶媒HCID 3283Diethyl Ether溶媒HCID 6569Methyl Ethyl Ketone溶媒HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A mixture of 0.556 g (1.57 mmol) of 7-[(5-bromopentyl)oxy]-2,3-dihydro-8-propyl-4H-1-benzopyran-4-one, 0.323 g (1.57 mmol) of 7-hydroxy-2-benzofurancarboxylic acid ethyl ester, 0.866 g (6.26 mmol) of anhydrous granular potassium carbonate and 16 mL of 2-butanone was stirred and refluxed for 16.5 hrs. The resulting slurry was filtered with suction and the solids were washed thoroughly with ethyl acetate. The filtrate and washes were combined and concentrated in vacuo and the residue was purified by flash chromatography on 70 g of silica gel, eluting with 4:1 hexane-ethyl acetate giving 0.527 g (70%) of 7-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acid ethyl ester as a white solid, mp 79.5°-81° C. A mixture of 0.262 g (0.55 mmol) of this ester in 3.5 mL of THF and 3.5 mL of water was treated with 35.1 mg (0.84 mmol) of lithium hydroxide monohydrate and the mixture was stirred for 17.5 hr. After being acidified with 16 mL of 3N aqueous sulfuric acid, the resulting mixture was worked-up with ether and ethyl acetate in the usual manner. The crude product was recrystallized from hexane-ethyl acetate to give 0.185 g (74.9%) of the title compound as a white solid, mp 152°-153.5° C.

後処理

  1. temperaturerefluxed for 16.5 hrs
  2. filtrationThe resulting slurry was filtered with suction
  3. washthe solids were washed thoroughly with ethyl acetate
  4. concentrationconcentrated in vacuo
  5. customthe residue was purified by flash chromatography on 70 g of silica gel
  6. washeluting with 4:1 hexane-ethyl acetate giving 0.527 g (70%) of 7-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acid ethyl ester as a white solid, mp 79.5°-81° C
  7. stirringthe mixture was stirred for 17.5 hr
  8. customThe crude product was recrystallized from hexane-ethyl acetate

出典と根拠

ORDレコード
ord-9d69c55117a2426da35c84b996250309
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05273999

反応ノート

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