Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1-Benzothiophen-5-yl)ethan-1-ol | HCID 11983371 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21283460 | HCID 21283460 | 72.3% |
Reaction Steps
To a solution of NaH (60% oil dispersion, 2.4 g, 0.06 mol) in DMF (50 ml) heated at 60° C. with stirring under N2 was added dropwise a solution of 5-(2-hydroxyethyl)benzo[b]thiophene (8.9 g, 0.05 mol) in DMF (50 ml). After 1/2 hour, a solution of benzyl bromide (10.3 g, 7.2 ml, d=1.438, 0.06 mol) in DMF (50 ml) was added dropwise. After 15 hours, the solution was poured into H2O and the aqueous phase extracted with ethyl acetate (3×). The organic layers were backwashed with H2O saturated NaCl, dried, filtered and concentrated to dryness. The residue was chromatographed on silica gel and the product was eluted with 10% (V/V) ethyl acetate-hexane to yield 9.7 g (72%) of product. The material was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04788192 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-0fc98a57d0c145c98649b4e9d7d59ab8 |
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| Source note | uspto-grants-1988_11 |
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