HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35534Generated: October 29, 2026
3-Methoxymethoxy-2-phenyl-7-azabenzothiophene → HCID 14277636, compound
https://huagongshe.com/reaction/35534
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methoxymethoxy-2-phenyl-7-azabenzothiophene | HCID 14673818 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14277636 | HCID 14277636 | 84% |
Reaction Steps
A solution of 2.72 g (10.0 mmol) of 3-methoxymethoxy-2-phenyl-7-azabenzothiophene in 20 mL of dry tetrahydrofuran was cooled to -78° C. To this was added 11 mL of a 1.0M solution of t-butyllithium in hexane and the solution was allowed to warm to room temperature. The solution was quenched with methanol and stirred in air for 60 minutes, then partitioned between ether and water. The aqueous layer was washed with two portions of ether and the combined extracts were washed with brine, dried, and concentrated to an oil. The oil was dissolved in 10 mL methanol and 10 mL of 2M HCl and stirred at room temperature for 24 hours. The solution was partitioned between ether and water and the ether layer dried and concentrated. Recrystallization from ether-hexane afforded 2.43 g (84%) of pale yellow needles, m.p. 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04767766 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-6e71c9af04b14b70a58865887b392b4a |
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| Source note | uspto-grants-1988_08 |
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