Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748769Generated: October 29, 2026

Toluene → HCID 59750703, compound

https://huagongshe.com/reaction/748769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantDiphenylphosphoryl azideHCID 123414—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 59750892HCID 59750892—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 59750703HCID 5975070358%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere and at 0° C., triethylamine (81.5 μl, 0.586 mmol) and diphenylphosphoric azide (126 μl, 0.586 mmol) were added to a toluene solution (5 ml) of the 4-[(4-chlorophenyl)sulfonyl]-4-(2,5-difluorophenyl)butyric acid (200 mg, 0.533 mmol) obtained in Example 200, followed by stirring at 0° C. for 2 hours. The reaction mixture was heated under reflux for 3 hours. After cooling to room temperature and addition of ethanol (2 ml), the mixture was heated under reflux for further 2 hours. The reaction mixture was then concentrated. The residue thus obtained was dissolved in dichloromethane. The resulting solution was washed successively with a saturated aqueous solution of potassium bicarbonate, water and brine, dried over magnesium sulfate and then, concentrated. The residue thus obtained was subjected to flash chromatography on a silica gel column, and the fraction obtained from the hexane:ethyl acetate=1:3 eluate was concentrated. The solid thus obtained was recrystallized from ethyl acetate-hexane, whereby the title compound (129 mg, 0.309 mmol, 58%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399775B2
Source datasetuspto-grants-2008_07
ORD IDord-ca61ff4e12184a919c43d6c7420a6afb
Source noteuspto-grants-2008_07