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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620911Generated: October 27, 2026

(-)-Asparagine → FMOC-L-asparagine

https://huagongshe.com/reaction/620911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(-)-AsparagineHCID 6267—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
ReactantDiisopropylethylamineHCID 81531—
ProductFMOC-L-asparagineHCID 2724774—

Reaction Steps

4.95 g (37.5 mmoles) of finely ground asparagine (Chemical Dynamics Corp.) was placed in a 250 mL round bottom flask (oven dried) which was fitted with a condenser (oven dried). A nitrogen gas line was attached at the top of the condenser. The solid was suspended in 87.5 mL of dry N,N-dimethylacetamide and stirred vigorously. 19.04 mL (150 mmoles) of Tms-Cl was injected in one portion. The mixture was stirred for 1 hour and cooled in an ice bath. 9-Fluorenylmethyoxycarbonyl chloride (6.47 g, 25 mmoles) and 19.78 mL (175 mmoles) of diisopropylethylamine were added. The solution was stirred in ice for 20 minutes and warmed to room temperature for 1-1.5 hrs. The mixture was concentrated on a rotary evaporator and then distributed between 200 mL diethyl ether and 250 mL 2.5% sodium bicarbonate. The phases were separated and the aqueous layer was extracted with 2×50 mL diethyl ether. The ether layers were backwashed with 2×25 mL H2O. The combined aqueous layers were acidified to pH 2 with 1.0N HCl. The white precipitate was filtered and washed with cold H2O. The product was then dried overnight. Appropriate solvents were used to recrystallize the product. The product was found to be homogeneous (Table II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822890
Source datasetuspto-grants-1989_04
ORD IDord-ee645d92ff64436f989046ed88e218e9
Source noteuspto-grants-1989_04