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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110189Generated: October 25, 2026

Triethylamine → Fmoc-Asn(Trt)-OH

https://huagongshe.com/reaction/1110189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantPotassium bisulfateHCID 516920—
ReactantN-(Triphenylmethyl)-L-asparagineHCID 7408309—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductFmoc-Asn(Trt)-OHHCID 640248—

Reaction Steps

3.4 g of 9-fluorenylmethyl N-succinimidyl carbonate (10 mmol) are added and, at the same time, 1.4 ml of triethylamine are added dropwise so that the pH is 8.3-8.7 to a vigorously stirred solution of 3.8 g of H-Asn(Trt)-OH.0.5 H2O (10 mmol) in 20 ml of tetrahydrofuran, 10 ml of water and 1.4 ml of triethylamine (10 mmol). After 20 minutes, the mixture is cooled in an ice bath and ethyl acetate and 25 ml of a one-molar aqueous potassium bisulfate solution are added. The organic phase is washed with water until free of sulfate, dried over sodium sulfate and concentrated under reduced pressure to about 50 g. The Fmoc-Asn(Trt)-OH can be crystallized by slow addition of diisopropyl ether, m.p. 210°-211° (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324833
Source datasetuspto-grants-1994_06
ORD IDord-6029d284f51645518896ddc67f84ada4
Source noteuspto-grants-1994_06