Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507891Generated: October 26, 2026

N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine → (4S,5R)-3-dichloroacetyl-2,2-dimethyl-4-fluoromethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine

https://huagongshe.com/reaction/507891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
ReactantHCID 25176380HCID 25176380—
SolventDichloromethaneHCID 6344—
Product(4S,5R)-3-dichloroacetyl-2,2-dimethyl-4-fluoromethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidineHCID 68470341—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

(4R,5R)-3-dichloroacetyl-2,2-dimethyl-4-hydroxymethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine (Compound XIIa) (81 g, 0.2050 moles) in methylene chloride (450 ml) reacts with N,N-diethyl-1,1,2,3,3,3-hexafluoro-1-propanamine (Ishikawa Reagent) (73.2 g, 0.328 moles) at 95-105° C. for 2-4 hours. Cooling to 20-25° C., quenching with 25% aqueous sodium hydroxide and water (2000 mL) and separation of the methylene chloride layer gives a solution of (4S,5R)-3-dichloroacetyl-2,2-dimethyl-4-fluoromethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine (Compound XIIIa) for use as an intermediate for the next step in the process.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786329B2
Source datasetuspto-grants-2010_08
ORD IDord-cbc958a226b7434db4b1300775c2dbfd
Source noteuspto-grants-2010_08