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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575500Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 71245667, compound

https://huagongshe.com/reaction/575500

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHexaneHCID 8058—
Reactant2-Butyl-1-octanolHCID 19800—
ReactantHCID 71245552HCID 71245552—
SolventMethylenechloride HexaneHCID 21226440—
ProductHCID 71245667HCID 7124566768.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

Compound 7 (1.80 g, 6.0 mmol), 1.14 g (6.0 mmol) of toluene-4-sulfonic acid (CH3C6H4SO3H.H2O), and 35 mL of 2-butyloctanol were added into a 250 mL 3-neck flask equipped with a ondenser. The system was heated at 180° C. overnight under argon before the mixture was cooled down to room temperature. Hexane (200 mL) was added and the organic layer was washed with saturated NaHCO3 before the solvent was removed under vacuum. Excess 2-butyloctanol was distilled out under vacuum. Column chromatography (silica gel) with an eluent of hexane/dichloromethane (v/v, 100/4) yielded product BB-4 as a colorless liquid (2.5 g, ˜68.5% yield). 1H NMR (CDCl3, 500 MHz): δ 7.96 (d, 2H, J=5.5 Hz), δ 7.60 (d, 2H, J=5.5 Hz), δ 7.50 (s, 2H), δ 4.23 (d, 4H, J=5.5 Hz), δ 1.99 (m, 2H), δ 1.33 (m, 32H), δ 0.96 (t, 6H, J=7.0 Hz), δ 0.90 (t, 6H, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035004B2
Source datasetuspto-grants-2015_05
ORD IDord-bf230322e9ab46d48f7cc0fca0d8ab85
Source noteuspto-grants-2015_05