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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097813Generated: October 29, 2026

Dimethyl Sulfoxide → 9-Bromononanal

https://huagongshe.com/reaction/1097813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Nonanol, 9-bromo-HCID 108700—
SolventDichloromethaneHCID 6344—
Product9-BromononanalHCID 54333081%

Reaction Conditions

Temperature-15 °C

Reaction Steps

9-Bromononan-1-ol (3 g. 13.4 mmol) was dissolved in dichloromethane (70 mL, 0.2M) and to this solution were added dimethyl sulfoxide (2.9 mL, 40.3 mmol) and diisopropylethylamine (7.0 mL, 40.3 mmol). The flask was then sealed under nitrogen and cooled to −15° C. Pyridine sulfur trioxide complex (6.4 g, 40.3 mmol) was added in two equal portions over 2 minutes and the resulting mixture was stirred at temperature between −10° C. and −20° C. for 30 minutes. The reaction was then quenched by adding water and the layers were separated. The organic layer was washed with aqueous sodium bisulfate (1M×3) and brine (×1), and then dried over magnesium sulfate, filtered and concentrated under reduced pressure to give the title compound as an amber oil (2.4 g 81% yield). 1H NMR (CDCl3, δ): 9.78 (s, 1H), 3.40 (t, 2H), 2.43 (t, 2H), 1.85 (m, 2H), 1.63 (m, 2H), 1.5-1.25 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143277B2
Source datasetuspto-grants-2012_03
ORD IDord-f981e7d826c84ab7b4ab3daec3799c16
Source noteuspto-grants-2012_03