Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-(N,N-diethylcarbamoyloxy)-6-methoxytoluene | HCID 59439476 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59439469 | HCID 59439469 | — |
Reaction Steps
5.0 mL of lithium diisopropylamide (2M/tetrahydrofuran-ethylbenzene, 10 mmol) was stirred and cooled on dry ice-ethanol bath and 8.0 mL tetrahydrofuran solution containing 0.95 g (4.0 mmol) of 2-(N,N-diethylcarbamoyloxy)-6-methoxytoluene was added dropwise thereto over 16 minutes. After one minute, warming was started under room temperature and after the mixture was stirred for 47 minutes, it was allowed to stand overnight. 10 mL of toluene and 10 mL of water were added thereto and after the mixture was stirred for 4 minutes, it was transferred into a separatory funnel and settled. The aqueous layer was separated and collected and combined with aqueous layers extracted from the organic layer with 2 N potassium hydroxide aqueous solution twice (5.0 mL for each time). After this aqueous layer was washed with 10 mL of toluene, 10 mL of toluene was added therein and 20 mL of 2 N hydrochloric acid aqueous solution was added thereto while being stirred and the mixture was transferred into a separatory funnel and settled. The organic layer was separated and collected and combined with the organic layer extracted from the aqueous layer with 5 mL of toluene. This organic layer was washed with 5 mL of water twice and then concentrated in vacuo, and thereby 0.81 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110688B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-c990343181af4bfaa4147ef14cfa493e |
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| Source note | uspto-grants-2012_02 |
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