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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047348Generated: October 30, 2026

Diisopropylethylamine → HCID 58388237, compound

https://huagongshe.com/reaction/2047348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11041660HCID 11041660—
ReactantHCID 58388236HCID 58388236—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductHCID 58388237HCID 5838823717.49%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4R)-3-[3-(3,4-difluorophenyl)propanoyl]-4-(phenylmethyl)-1,3-oxazolidin-2-one (1 g, 2.90 mmol) in dichloromethane (29.0 ml) at −60° C. was added TiCl4 (0.335 ml, 3.04 mmol) dropwise. After 30 min, DIPEA (0.556 ml, 3.19 mmol) was added and the solution stirred at 1 h at 0° C. phenylmethyl [(methyloxy)methyl]carbamate (1.131 g, 5.79 mmol)[prepared according to Barnett, C. J. et al, Tetrahedron Lett. 1997, 38, 5, 735.] was added and the reaction mixture stirred at 0° C. for 4 h. The solution was quenched with aqueous saturated ammonium chloride solution and extracted several times with DCM. The combined organic fractions were dried over Na2SO4, concentrated and purified by column chromatography (0-50% EtOAc in hexanes) affording phenylmethyl {(2S)-2-[(3,4-difluorophenyl)methyl]-3-oxo-3-[(4R)-2-oxo-4-(phenylmethyl)-1,3-oxazolidin-3-yl]propyl}carbamate (548 mg, 0.506 mmol, 17.49% yield) as a clear oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592475B2
Source datasetuspto-grants-2013_11
ORD IDord-519c0e7b8ea641059d868fe6bb2f9a6d
Source noteuspto-grants-2013_11