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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625645Generated: October 30, 2026

N-(9-Fluorenylmethoxycarbonyloxy)succinimide → Fmoc-L-Prolinol

https://huagongshe.com/reaction/1625645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantL-ProlinolHCID 640091—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductFmoc-L-ProlinolHCID 68863574%

Reaction Steps

L-prolinol (Compound 1) (0.61 g, 6.0 mmol) was dissolved in 70 ml of pure water, thus preparing an L-prolinol aqueous solution. N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-OSu) (2.0 g, 6.0 mmol) was dissolved in 10 ml of THF. This THF solution was added to the L-prolinol aqueous solution, and this was stirred for 1 hour so as to react the L-prolinol and the Fmoc-OSu. The reaction solution was separated into a liquid fraction and a precipitate fraction. These fractions respectively were subjected to extraction with ethyl acetate, and organic layers respectively were collected therefrom. The thus-obtained organic layers were mixed together, and anhydrous sodium sulfate was added thereto to absorb moisture (hereinafter, this process is referred to as a “drying” process). The organic layers were filtered, and the filtrate obtained was vacuum concentrated. The residual substance obtained was purified by silica gel column chromatography (the eluent: hexane:ethyl acetate=1:1). Thus, Compound 2 was obtained (1.4 g, yield: 74%). The result of NMR analysis with respect to this compound is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785121B2
Source datasetuspto-grants-2014_07
ORD IDord-e910b27c1793489d9374073a27f637c9
Source noteuspto-grants-2014_07