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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472247Generated: October 31, 2026

1,3,5-Trioxane → (S)-4-Benzyl-3-((R)-2-hydroxymethyl-4-methylpentanoyl)oxazolidin-2-one

https://huagongshe.com/reaction/1472247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-TrioxaneHCID 8081—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-4-Benzyl-3-(4-methylpentanoyl)oxazolidin-2-oneHCID 10869526—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product(S)-4-Benzyl-3-((R)-2-hydroxymethyl-4-methylpentanoyl)oxazolidin-2-oneHCID 5955678398.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Intermediate (2a) (14.5 g, 46.3 mmol) was dissolved in DCM (151 mL, 2.4 mol) and stirred at 0° C. under nitrogen. 1M titanium tetrachloride in DCM (48.6 mL) was added and stirred for 15 minutes. DIPEA (8.9 mL, 51.0 mmol) was added dropwise at 0° C. and the mixture was stirred for 75 minutes. 1,3,5-Trioxane (4.6 g, 51.0 mmol) in DCM (30 mL) was then added. After 10 minutes a second equivalent of 1M titanium tetrachloride in DCM (48.6 mL) was added and the mixture stirred at 0° C. for 5 hours. The reaction was then quenched with 250 mL of saturated ammonium chloride. Water and DCM were added, and the aqueous phase was extracted twice more with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated. The resulting material was purified by silica gel chromatography (0-60% EtOAc:hexanes) to provide intermediate (2b) (13.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012485B2
Source datasetuspto-grants-2015_04
ORD IDord-3548f8e5f1a4493e8cecb7a7cd745965
Source noteuspto-grants-2015_04