HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613601Generated: October 30, 2026
Tetrabutylammonium Fluoride Trihydrate → 7-Nitro-trans-5-(5-chloro-1,2-dihydro-2-oxo-pyrid-1-yl)-2,3,4,5-tetrahydro-1-benzoxepin-4-ol
https://huagongshe.com/reaction/1613601
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Reactant | 4,5-Epoxy-7-nitro-2,3,4,5-tetrahydro-benzoxepin | HCID 14580522 | — |
| Reactant | 5-Chloro-2-trimethylsilyl-pyridine | HCID 15169006 | — |
| Product | 7-Nitro-trans-5-(5-chloro-1,2-dihydro-2-oxo-pyrid-1-yl)-2,3,4,5-tetrahydro-1-benzoxepin-4-ol | HCID 67883728 | — |
Reaction Steps
6.63 g (21 mmol) of tetrabutylammonium fluoride trihydrate are added to a stirred mixture of 3.93 g (19 mmol) of 4,5-epoxy-7-nitro-2,3,4,5-tetrahydro-1-benzoxepin and 8.06 g (40 mmol) of 5-chloro-2-trimethylsilyl-pyridine, and the mixture is heated at 60° C. for 5 hours. The mixture is then stirred into ice-water and extracted several times with ethyl acetate. The combined ethyl acetate extracts are washed with water and saturated sodium chloride solution dried over sodium sulfate, filtered and evaporated in vacuo. The remaining viscous oil crystallizes after standing for some time. It is triturated with ethyl acetate and filtered off with suction. Crystals of melting point 219°-222° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05194442 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-ec2cea65ada8406289989e264b095ac0 |
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| Source note | uspto-grants-1993_03 |
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