Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86597999 | HCID 86597999 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86597998 | HCID 86597998 | — |
Reaction Steps
A mixture of (44) (936 mg, 4.76 mmol), pivalic acid (2.43 g, 23.8 mmol) and N,N-diisopropylethylamine (2.40 g, 23.8 mmol) was stirred at 75° C. for four days, and the reaction was judged complete by 1H-NMR. The reaction mixture was cooled to room temperature and portioned between water and ether, the ether phase was washed successively with water, aqueous NaHCO3, and brine, then dried over anhydrous Na2SO4. After rotary evaporation, the crude O-(1-pivaloyloxyisobutoxy) S-ethyl thiocarbonate (45) was obtained in quantitative yield, and used in the next step without further purification. 1H NMR (CDCl3, 400 MHz): δ 0.96 (d, 6H), 1.21 (d, 9H), 1.30 (t, 3H), 2.03 (m, 1H), 6.65 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572830B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-178af6967d844749875cace7b192550f |
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| Source note | uspto-grants-2009_08 |
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