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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754820Generated: October 28, 2026

Toluene → N-Fmoc-di(4-docosoxyphenyl)methylamine

https://huagongshe.com/reaction/1754820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethanesulfonic AcidHCID 6395—
ReactantBenzhydrolHCID 7037—
ReactantSodium BicarbonateHCID 516892—
Reactant9-Fluorenylmethyl carbamateHCID 736301—
Reactant4,4'-DidocosoxybenzhydrolHCID 46936142—
ProductN-Fmoc-di(4-docosoxyphenyl)methylamineHCID 8664619560%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 4,4′-didocosoxybenzhydrol (713 mg, 856 μmol) were added toluene (15 ml), Fmoc-NH2 (246 mg, 1.03 mmol) and methanesulfonic acid (8.3 μl, 128 μmol), and the mixture was stirred at 100° C. for 3 hr. After confirmation of disappearance of a benzhydrol type anchor, the mixture was cooled to room temperature. 2.5% Aqueous sodium hydrogen carbonate (10 ml) was added and the mixture was stirred. After partitioning, the organic layer was further washed with water (10 ml×2). The organic layer was evaporated under reduced pressure, and the residue was washed with methanol (10 ml) to give N-Fmoc-di(4-docosoxyphenyl)methylamine (540 mg, 512 μmol, yield 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169187B2
Source datasetuspto-grants-2015_10
ORD IDord-0a0723aaf2904560bba542791cd066a1
Source noteuspto-grants-2015_10