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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263083Generated: November 2, 2026

12-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl ether → 12-fluoro-(Z)-3-dodecen-1-ol

https://huagongshe.com/reaction/1263083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant12-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl etherHCID 13372592—
SolventMethanolHCID 887—
Product12-fluoro-(Z)-3-dodecen-1-olHCID 8673950784.3%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 12-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl ether (0.5242 g, 1.83 mmol) (prepared as in Example 5 above) in methanol (10 ml) is added Dowex resin (0.5 g) and the mixture is heated at 45° C. overnight (Bongini et. al., Synthesis, 618, 1979). The resin is then filtered off and the solvent is removed in vacuo. The crude product is purified by flash chromatography using hexane/ethyl acetate (93:7, v/v) to give 12-fluoro-(Z)-3-dodecen-1-ol (312 mg, 83%) as a clear colorless oil: Rf=0.36, hexane/ethyl acetate (7:3, v/v); IR (film ν3100-3550 (OH), 3000 (C=CH); and H NMR (CDCl3) δ1.25-1.75 (m, 12H), 2.15 (m, 2H), 2.35 (br q, J=6 Hz, 2H), 3.65 (t, J=9 Hz, 2H), 4.41(dt, J=48 Hz, 6 Hz, 2H), 5.46 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04455441
Source datasetuspto-grants-1984_06
ORD IDord-c5d003f873724ca6b7f3080bf1e4a7bc
Source noteuspto-grants-1984_06