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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722801Generated: October 30, 2026

Iodine → (2S,3R)-2-(N,N-Dibenzylamino)-3-tetradecanol

https://huagongshe.com/reaction/722801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-BromoundecaneHCID 12744—
Reactant(S)-2-Dibenzylamino-propionaldehydeHCID 11107860—
SolventTetrahydrofuranHCID 8028—
Product(2S,3R)-2-(N,N-Dibenzylamino)-3-tetradecanolHCID 5874337244.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of Mg (155 mg, 6.38 mmol) and a few crystals of I2 in THF (3.1 mL), an aliquot of 1-bromoundecane (0.25 mL, 1.12 mmol) was added and the mixture was stirred at 60° C. until the red color of the solution disappeared. Then the remainder of 1-bromoundecane (0.46 mL, 2.07 mmol) was added and the reaction was stirred at room temperature for 1 h. The Grignard solution formed thereof was cooled down to 0° C. and a solution of aldehyde 4 (323.5 mg, 1.28 mmol) in THF (1.6 mL) was added via cannula. After stirring overnight at room temperature, the reaction was quenched with HCl (3N, 10 mL) extracted with EtOAc (3×10 mL), washed successively with NaHCO3 (20 mL, sat. aq.) and brine (20 mL), dried over Na2SO4 and concentrated in vacuo. The crude was purified by column chromatography on silica (100% hexane to 10:1 hexane/EtOAc) to obtain a mixture of diastereoisomers. Further purification by HPLC on silica (95:5 to 80:20 hexane/MTBE) afforded pure anti alcohol 29 as a colorless oil (205 mg, 39% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138547B2
Source datasetuspto-grants-2006_11
ORD IDord-fbb3599bbaef4aa488aa47537434fcf5
Source noteuspto-grants-2006_11