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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373140Generated: October 25, 2026

Water → 4-Butylthiobenzaldhyde

https://huagongshe.com/reaction/2373140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
Reactant(4-Bromophenyl)(butyl)sulfaneHCID 14418074—
ReactantButyllithiumHCID 178418339—
Product4-ButylthiobenzaldhydeHCID 19091707—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromophenyl n-butyl sulfide (1.5 g, 6.12 mmol) in 60 ml of dry THF was added nBuLi (4.1 ml, 1.6 M in hexanes) at −78° C. under nitrogen. The mixture was stirred for 1 hour at −78° C. and then DMF (2.0 ml) was added. The reaction mixture was stirred at room temperature for 2 hours. Then 40 ml of water was added to this mixture, the product was extracted three times by ether (3×50 ml) and the combined organic layer was dried over magnesium sulfate. After removal of solvent under reduced pressure, the product was purified by flash chromatography column using 10% of ethyl acetate in hexanes as eluant and isolated in 66.7% (0.88 g) yield.1H NMR (CDCl3, 500 MHz) δppm: 9.98 (s, 1H, CHO), 7.77 (d, J=8.5 Hz, 2H), 7.36 (d, J=8.5 Hz, 2H,), 7.11 (s, 2H), 3.02 (t, J=7.2 Hz, 2H, CH2), 1.71 (m, 2H, CH2), 1.50 (m, 2H, CH2), 0.97 (t, J=7.5 Hz, 6H, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459106B2
Source datasetuspto-grants-2008_12
ORD IDord-77d3a63bde484380b78001c4be4e39ec
Source noteuspto-grants-2008_12