HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34609Generated: October 30, 2026
Diethyl Ether → 4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcohol
https://huagongshe.com/reaction/34609
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-[4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyloxy]-tetrahydropyran | HCID 13911481 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcohol | HCID 13911482 | — |
Reaction Steps
The crude tetrahydropyranyl ether prepared in Stage (i) was dissolved in methanol (20 cm3), and to the stirred solution was added concentrated hydrochloric acid (3 drops). After stirring for 16 hours at the ambient temperature (ca. 25° C.), the reaction mixture was poured into ethyl acetate, washed with water and brine, and dried. Evaporation of the solvent under reduced pressure gave a yellow oil which was subjected to column chromatography on silica gel using petroleum ether (boiling range 40°-60° C.) containing diethyl ether (10% gradually increased to 40% by volume) as eluent to give 4-trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcohol (0.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762835 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-c63bc3ba6643468999e4739e9fb348d1 |
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| Source note | uspto-grants-1988_08 |
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