Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Alpha-Methylstyrene | HCID 7407 | — |
| Reactant | Lauryl Methacrylate | HCID 8906 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178506801 | HCID 178506801 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Lauryl Methacrylate | HCID 8906 | — |
| Product | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
Reaction Steps
Under a high vacuum, a tetarahydrofuran solution of sodium salt of a-methylstyrene tetramer was introduced into a polymerization vessel, and removed after sufficiently washing the vessel. Then, 198 ml of tetrahydrofuran and 18 ml (3.0 mmole) of a benzene solution of 1,1-diphenylhexyl lithium were introduced under the room temperature into the vessel, which in turn was cooled to -78° C. Then, 111 ml (74 mmole) of a tetrahydrofuran solution of n-lauryl methacrylate was introduced into the vessel to start polymerization. After a lapse of 2 hours, the mixture was further stirred for 30 minutes with introduction of 95 ml (66 mmole) of a tetrahydrofuran solution of 3-methacryloylethoxydimethylisopropylsilane, thereafter the reaction was stopped with addition of 2 ml of methanol, and 1 ml of 2N-hydrochloric acid was added into the reaction vessel to obtain a block polymer of poly n-lauryl methacrylate and polyhydroxyethyl methacrylate. After the reaction was finished, the solvent was removed so that the nonvolatile content was 50%. Hydrophobic and hydrophilic blocks forming this block polymer exhibited molecular weights of 2410 and 1210 respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05603986 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-a7e790b7600a4e25951ef7cdaee697c8 |
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| Source note | uspto-grants-1997_02 |
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