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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098673Generated: October 25, 2026

Aniline → HCID 59593434, compound

https://huagongshe.com/reaction/1098673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTrimethylaluminumHCID 16682925—
Reactant(R)-3-(tert-butyldiphenylsilyloxy)dihydrofuran-2(3H)-oneHCID 53797635—
ReactantHCID 86590012HCID 86590012—
SolventDichloromethaneHCID 6344—
ProductHCID 59593434HCID 5959343478.4%

Reaction Steps

To a solution of aniline (356 mg, 348 μL, 3.82 mmol) in DCM (17 mL) was added trimethylaluminum (2.0M, 2.1 mL, 4.2 mmol) dropwise and the reaction mixture was stirred at RT for 40 min. A solution of (R)-3-(tert-butyldiphenylsilyloxy)-dihydrofuran-2(3H)-one (1.00 g, 2.94 mmol) in DCM (12 mL) was added dropwise and the reaction mixture was stirred at RT for 16 hours. The reaction mixture was poured into a saturated solution of sodium potassium tartaric acid and stirred for 15 min. The layers were separated, and the aqueous layer was washed with DCM (4×). The combined organics were washed with 0.1M HCl (2×), brine, dried over Na2SO4 and evaporated to dryness. Purification by silica gel chromatography (10-30% EtOAc in hexane) afforded the (R)-2-(tert-butyldiphenylsilyloxy)-4-hydroxy-N-phenylbutanamide (1.00 g, 78%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=434.7; tR=2.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143297B2
Source datasetuspto-grants-2012_03
ORD IDord-1bbae4d73c0c41c8a7bc126a54e61afa
Source noteuspto-grants-2012_03