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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342876Generated: October 30, 2026

1,2-Dichloroethane → HCID 7033973, compound

https://huagongshe.com/reaction/342876

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAnilineHCID 6115—
ReactantPentafluorophenolHCID 13041—
ReactantBenzyloxycarbonyl-L-phenylalanineHCID 70878—
SolventDichloromethaneHCID 6344—
ProductHCID 7033973HCID 7033973—

Reaction Conditions

Temperature0 °C

Reaction Steps

Nα -Benzyloxycarbonyl-L-phenylalanine (4.95 g, 16.5 mmol) was dissolved in dichloromethane (70 ml) and the solution was cooled to 0° C. and stirred during the addition of pentafluorophenol (3.35 g, 18.2 mmol), followed by EDC (3.49 g, 18.2 mmol). The mixture was allowed to warm to room temperature, stirred for a further 1 hour then cooled back to 0° C. Aniline (3.85 g, 41.4 mmol) was added dropwise and the mixture was warmed to room temperature then stirred overnight. The solution was washed twice with 1M sodium carbonate, twice with 1M hydrochloric acid and finally with brine before drying over anhydrous magnesium sulphate. The solution was filtered and evaporated to a white solid which was recrystallised from ethyl acetate-hexane. Yield: 2.57 g (41%). 1H-NMR; δ (CDCl3), 7.87 (1H, brs), 7.43-7.03 (15H, br m), 5.62 (1H, m), 5.08 (2H, s), 4.59 (1H, s) and 3.15 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859253
Source datasetuspto-grants-1999_01
ORD IDord-e30f50bb72ae4626b97ddf254cb972c7
Source noteuspto-grants-1999_01