HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591503Generated: October 30, 2026
Tetrahydrofuran → HCID 89768078, compound
https://huagongshe.com/reaction/591503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 89767964 | HCID 89767964 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 89768078 | HCID 89768078 | 12.4% |
Reaction Steps
To a mixture of 2-(6-((2,4-dichlorobenzyl)oxy)-1-benzothiophen-3-yl)acetamide (73.3 mg) and THF (dry) (10 mL) was added sodium bis(trimethylsilyl)amide (0.158 ml, 1.9 M in toluene) at −78° C. The mixture was stirred at −40° C. under argon atmosphere for 30 min. And then methanesulfonyl chloride (34.4 mg) was added thereto. The resulting mixture was stirred at room temperature under argon atmosphere overnight. The mixture was poured into water and extracted with EtOAc. The organic layer was separated, washed successively with water and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (11.00 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238639B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-6c2c50998dce4d949a6e4dc2286ecea1 |
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| Source note | uspto-grants-2016_01 |
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