Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 58168619 | HCID 58168619 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58168596 | HCID 58168596 | — |
Reaction Steps
A solution of acetyl chloride (0.36 mL) in dry THF (3 mL) was added dropwise over 10 minutes to a stirred solution at 20° C. of 2-(4-(2-(tert-butyldimethylsilyloxy)ethyl)thiophen-2-yl)ethanol [Aromatic Intermediate 20] (1.10 g) and triethylamine (1.18 mL) in dry THF (30 mL). The mixture was stirred at 20° C. for 20 minutes and then partitioned between ethyl acetate and brine. The organic layer was dried, filtered and the solvent evaporated under reduced pressure to give the subtitled compound. Yield 1.20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455483B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-a3d3dd5c26ed485f8d9c295ee87ca5f5 |
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| Source note | uspto-grants-2013_06 |
|---|