Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Benzothiazole, 2,6-dimethyl- | HCID 76253 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12016698 | HCID 12016698 | 61% |
Reaction Steps
A solution of 2,6-dimethylbenzothiazole (13.0 g) and 2-bromoethanol (100 g) was stirred and heated in an oil bath to 120° C. for 96 hours. After cooling the reaction mixture to room temperature, adding ethyl acetate (150 ml) and stirring for 1 hour, the resultant solid was filtered and collected. The solid was then dissolved in methanol (150 ml) and charcoal (2 g) was added. The charcoal was removed by passing through a pad of Celite®. The solution was then concentrated to a small volume and triturated with acetone (200 ml). The solid was collected, washed with acetone (2×30 ml), ethyl acetate (2×30 ml) and dried in an oven under high vacuum at 50 C overnight to obtain 13.95 g (61%) of 4b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06551831B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-bca1855b717c479a8da8761348ec737a |
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| Source note | uspto-grants-2003_04 |
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