HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222415Generated: November 1, 2026
Trifluoroacetic acid methylene chloride → HCID 69134812, compound
https://huagongshe.com/reaction/2222415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Reactant | HCID 69135032 | HCID 69135032 | — |
| Product | HCID 69134812 | HCID 69134812 | — |
Reaction Steps
4-(2-tert-Butoxyethoxy)tetrahydropyran (24 g, 0.12 mol) was stirred in a mixture of methylene chloride/trifluoroacetic acid (150 ml/150 ml) at ambient temperature overnight. The solvents were evaporated off and the residual trifluoroacetic acid was azeotroped off with, toluene. The crude oil was purified by flash chromatography using successively petroleum ether, petroleum ether/methylene chloride (1/1) and methylene chloride. The organic phase was washed with water, brine, dried (MgSO4), filtered and the solvent evaporated. Evaporation of the solvent gave 4-(2-trifluoroacetoxyethoxy)tetrahydropyran which was hydrolysed with potassium hydrogen carbonate (48 g, 0.48 mol) in methanol (700 ml) and water (300 ml) at ambient temperature for 3 hours. The solution was neutralised to pH 7 and the solvents evaporated off. The residue was extracted with ethyl acetate, the organic phase washed with water and brine, dried (MgSO4) and the solvent evaporated off to give 4-(2-hydroxyethoxy)tetrahydropyran (6 g, 35%) as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371765B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-f4df2c5f151545ef9777da2c507ea102 |
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| Source note | uspto-grants-2008_05 |
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