Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Tin atom | HCID 5352426 | — |
| Reactant | HCID 15481279 | HCID 15481279 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15481240 | HCID 15481240 | 63% |
Reaction Steps
To a cold (-78° C.) solution of 2-(3-methoxybenzyl)-benzo[b]thiophene (2.10 g, 8.26 mmol) and p-anisoyl chloride (1.48 g, 8.67 mmol) in anhydrous methylene chloride (31 mL) was added tin IV chloride (2.90 mL, 24.8 mmol, 3 eq) dropwise over a period of 24 minutes. After stirring overnight in the warming dry ice bath and at ambient temperature for 7 hours the reaction mixture was poured onto water (175 mL) and the organics were extracted with diethyl ether (2×300 mL). The extracts were combined, and washed with brine. Silica gel was added and the solvent was removed. The adsorbate was flash chromatographed (97/3 petroleum ehter/ethyl acetate) to give the title compound as a white solid (1.92 g, 63%): mp 158-159° C.; MS (+FAB): [M+] 370; Anal. Calc. for C24H18O2S: C, 77.81, H, 4.90, N, 0.00. Found: C, 78.00, H, 4.76, N, 0.03.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06110962 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-a18afcd929e5455fa655a1799be46230 |
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| Source note | uspto-grants-2000_08 |
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