Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57368066 | HCID 57368066 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzoin | HCID 8400 | — |
Reaction Steps
As shown in the following reaction 1, 30 g of benzoin acrylate, which is obtained from the reaction of benzoin and chloroacylate, and 1 L of chloroform were added into a 2 L reactor, and was stirred and cooled in iced water. 47 g of 3-chloroperoxybenzoicacid(mCPBA) were slowly added into the cooled solution, and the reaction was carried out at room temperature for 24 hours. After completion of the reaction, the 3-chlorobenzoicacid (by-product) was removed by filtering the product, and then the residual 3-chlorobenzoicacid was removed by washing 2 times with saturated sodium sulfite aqueous solution, 1 time with saturated sodium bicarbonate aqueous solution, 1 time with saturated sodium chloride aqueous solution, and 1 time with distilled water. Next, the product was dried with magnesium sulfate, and chloroform was removed under reduced pressure, and then the product was vacuum dried for 1 day to obtain 27.3 g of the pure benzoin acrylate oxide. NMR spectrum of the obtained benzoin acrylate oxide is described in FIG. 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07309561B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-db40a96cbf6f4165998b4e724bf6acb9 |
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| Source note | uspto-grants-2007_12 |
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