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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877405Generated: October 26, 2026

Thiazole → 7-Phenyl-1-(thiazol-2-yl)-heptan-1-ol

https://huagongshe.com/reaction/877405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
Reactant7-PhenylheptanalHCID 14840064—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-Phenyl-1-(thiazol-2-yl)-heptan-1-olHCID 5836626162.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Thiazole (21 μL, 0.29 mmol) in anhydrous THF (1.9 mL) was cooled to −78° C. and treated dropwise with 1.4 M t-BuLi (273 μL, 0.38 mmol). The reaction mixture was stirred at −78° C. for 0.5 h before a solution of 7-phenylheptanal (73 mg, 0.38 mmol) in THF (1.3 mL) was added. The reaction mixture was stirred at −78° C. for 0.5 h before being warmed to room temperature. The reaction mixture was diluted with EtOAc, and washed with H2O, saturated aqueous NaHCO3 and saturated aqueous NaCl before the organic layer was dried over Na2SO4 and the solvent was removed under reduced pressure. Flash chromatography (SiO2, 1.5×6.5 cm, 15-25% EtOAc-hexanes) afforded the title compound (50 mg, 62%) as a colorless oil: 1H NMR (CDCl3, 400 MHz) δ 7.68 (d, 1H, J=3.2 Hz), 7.24 (m, 3H), 7.14 (m, 3H), 4.96 (dd, 1H, J=4.8, 7.6 Hz), 3.09 (br s, 1H), 2.56 (t, 2H, J=7.8 Hz), 1.87 (m, 2H), 1.58 (m, 2H), 1.44 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987312B2
Source datasetuspto-grants-2015_03
ORD IDord-22c9ac5fc43d4225bb35b0a924152e94
Source noteuspto-grants-2015_03