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2-Methyltetrahydrofuran → 9H-Fluoren-9-YL acrylate

HRID 1013621
ノート
印刷プレビュー

反応式

HRID 1013621 の反応式
[OH:1][CH:2]1[C:14]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.C[CH:16]1[CH2:20][CH2:19]C[O:17]1.C(N(CC)CC)C.C(Cl)(=O)C=C>>[CH:13]1[C:14]2[CH:2]([O:1][C:16](=[O:17])[CH:20]=[CH2:19])[C:3]3[C:8](=[CH:7][CH:6]=[CH:5][CH:4]=3)[C:9]=2[CH:10]=[CH:11][CH:12]=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 73012-MethyltetrahydrofuranHCID 8471TriethylamineHCID 13140Acryloyl chlorideHCID 74318Fluoren-9-ol

生成物 1

HCID 579315729H-Fluoren-9-YL acrylate

実験手順

To a 250 ml 3 neck round bottom was added 9-Hydroxyfluorene (5 g, 0.027 mole, 1.0 equivalent), 2-methyltetrahydrofuran (50 g), triethylamine (3.3 g, 0.03 mole, 1.2 equivalents) and cooled in an ice bath. The cooled solution was treated with acryloyl chloride (2.7 g, 0.03 mole, 1.1 equivalents) dropwise over 1 hour. Analysis by gas chromatography indicated 60/40 mixture. The reaction was washed two times with sodium chloride brine (25 ml, 20% aqueous solution), concentrated invacuo to recover a solid. The material was dissolved in chloroform (50 ml) and added to a silica gel column containing 500 g silica gel and eluted with hexane/ethyl acetate at varying concentrations of 1-2.5% (ethyl acetate). The product was eluted first and was recovered by concentrating invacuo. Recovered 2.5 g of a pale yellow oil, which quickly solidified, having a melting point of 64-65 C. Polymerizable Resin Composition 1: 40 parts of FA-1 (with a refractive index of 1.613), 50 parts CN120 (epoxy acrylate available from Sartomer Company, Exton, Pa., reported by Sartomer to have a viscosity of 2150 cps at 65° C., a refractive index of 1.5556 and a Tg of 60° C.), 10 parts SR339(2-phenoxyethyl acrylate available form Sartomer), and 0.3 parts Darocur 4265 (available from Ciba Specialty Chemicals, Tarrytown, N.Y.) were mixed together thoroughly in an amber jar. Optical Film Sample Preparation: Brightness enhancing films samples were made using Polymerizable Resin Composition 1. About 3 grams of warm resin was applied to a 2 mil primed PET (polyester) film, available from DuPont under the trade designation “Melinex 623” and placed against a microstructured tool with a 90/24 pattern similar to the commercially available Vikuiti TBEF-90/24. The PET, resin and tool were passed through a heated laminator set at approximately 150° F. to create a uniformly thick sample. The tool containing the film and coated resin sample was passed at 50 fpm through a Fusion UV processor containing two 600 W/in D-bulbs. The PET and cured resin were removed from the tool and cut into samples. Gain Test Method

後処理

  1. temperaturecooled in an ice bath
  2. washThe reaction was washed two times with sodium chloride brine (25 ml, 20% aqueous solution)
  3. concentrationconcentrated invacuo
  4. customto recover a solid
  5. dissolutionThe material was dissolved in chloroform (50 ml)
  6. additionadded to a silica gel column
  7. additioncontaining 500 g silica gel
  8. washeluted with hexane/ethyl acetate
  9. washThe product was eluted first
  10. customwas recovered
  11. concentrationby concentrating invacuo
  12. customRecovered 2.5 g of a pale yellow oil, which
  13. customat 65° C.
  14. additiona refractive index of 1.5556 and a Tg of 60° C.), 10 parts SR339(2-phenoxyethyl acrylate available form Sartomer), and 0.3 parts Darocur 4265 (available from Ciba Specialty Chemicals, Tarrytown, N.Y.) were mixed together thoroughly in an amber jar
  15. customOptical Film Sample Preparation
  16. customset at approximately 150° F.
  17. additionThe tool containing the film and coated resin sample
  18. additioncontaining two 600 W/in D-bulbs
  19. customwere removed from the tool

出典と根拠

ORDレコード
ord-709ab6109fe349a7bfcbca75174c4a5f
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07981986B2

反応ノート

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