反応式
[CH:1](=[CH:10][C:11]([OH:13])=O)[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.S(Cl)([Cl:16])=O>CCCCCC>[CH:1](=[CH:10][C:11]([Cl:16])=[O:13])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
4
実験手順
Preparation of C6H5—CH═CH—CH═CH—CO2PEG—OCH2CH(OC2H5)2: A solution of cinnamylideneacetic acid (1.7 g, 0.01 moles) and thionyl chloride (3 ml, 0.04 moles) in 50ml of hexane were refluxed under N2 for 4 h, then filtered to remove a small amount of dark solid and the filtrate evaporated under vacuum. The residue was dried under vacuum overnight at room temperature to obtain 1.5 g of cinnamylideneacetyl chloride as a yellow solid, m.p. 51-52° C.)
後処理
- customPreparation of C6H5—CH═CH—CH═CH—CO2PEG—OCH2CH(OC2H5)2
- filtrationfiltered
- customto remove a small amount of dark solid
- customthe filtrate evaporated under vacuum
- customThe residue was dried under vacuum overnight at room temperature
出典と根拠
- ORDレコード
- ord-afa60633ca85481e8b51d5815ad025d2
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06864327B2
関連ノート
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