Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507885Generated: October 31, 2026

N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine → HCID 11336441, compound

https://huagongshe.com/reaction/507885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
ReactantHCID 11186465HCID 11186465—
SolventDichloromethaneHCID 6344—
ProductHCID 11336441HCID 11336441—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

(4R,5R)-3-acetyl-2,2-dimethyl-4-hydroxymethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine (Compound II) (75 g, 0.2291 moles) in methylene chloride (525 ml) reacts with N,N-diethyl-1,1,2,3,3,3-hexafluoro-1-propanamine (Ishikawa Reagent) (76.7 g, 0.3437 moles) at 95-105° C. for about 4 hours. Cooling to 20-25° C., addition to sodium hydroxide (6 g) in water (2500 mL), separation of the methylene chloride layer, distillation and replacement of methylene chloride by isopropanol (750 mL), precipitates the desired product. Filtration, washing with water (100 mL) and isopropanol (75 mL), then drying yields (4S,5R)-3-acetyl-2,2-dimethyl-4-fluoromethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine (Compound IX: R1 is methylsulfonyl; R2, R3 and R4 are methyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786329B2
Source datasetuspto-grants-2010_08
ORD IDord-5aa0627934d04c078d4b1422d3c90e58
Source noteuspto-grants-2010_08