2-Chloroethyl Benzenesulfonate → 5-(2-Chloroethoxy)benzo[b]thiophene-2-carboxylic acid methyl ester
反応式
[CH3:1][O:2][C:3]([C:5]1[S:9][C:8]2[CH:10]=[CH:11][C:12]([OH:14])=[CH:13][C:7]=2[CH:6]=1)=[O:4].C1(S(O[CH2:25][CH2:26][Cl:27])(=O)=O)C=CC=CC=1>[Na].CO>[CH3:1][O:2][C:3]([C:5]1[S:9][C:8]2[CH:10]=[CH:11][C:12]([O:14][CH2:25][CH2:26][Cl:27])=[CH:13][C:7]=2[CH:6]=1)=[O:4]参加物
実験手順
5-Hydroxybenzo[b]thiophene-2-carboxylic acid methyl ester (1.47 g.) was dissolved in a solution of sodium (0.163 g.) in methanol (15 ml.) and 2-(benzenesulphonyloxy)ethyl chloride (1.57 g.) was added. The resulting solution was heated under reflux for 8 hours and then allowed to cool and stood overnight. The solution was then evaporated and the residue was partitioned between water and ether. The aqueous layer was separated and washed several times with ether. The combined organic layer and ethereal extracts were washed with water, dried (Na2SO4) and evaporated. The residue was chromatographed on silica gel. Elution with chloroform gave a solid which was crystallized from ethyl acetate/petrol (b.p. 60°-80°) to give 5-(2-chloroethoxy)benzo[b]-thiophene-2-carboxylic acid methyl ester, (0.74 g.), m.p. 116°-117° C.
後処理
- additionwas added
- temperatureThe resulting solution was heated
- temperatureunder reflux for 8 hours
- temperatureto cool
- customThe solution was then evaporated
- customthe residue was partitioned between water and ether
- customThe aqueous layer was separated
- washwashed several times with ether
- washThe combined organic layer and ethereal extracts were washed with water
- dry with materialdried (Na2SO4)
- customevaporated
- customThe residue was chromatographed on silica gel
- washElution with chloroform
- customgave a solid which
- customwas crystallized from ethyl acetate/petrol (b.p. 60°-80°)
出典と根拠
- ORDレコード
- ord-263a9902110f4542aeb3a05a1f436f00
- 出典データセット
- uspto-grants-1983_10
- 特許番号
- US04410539
反応ノート
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