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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522862Generated: October 28, 2026

Hydrogen Bromide → (9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/522862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant9H-fluoren-9-ylmethyl-4-(diazoacetyl)piperidine-1-carboxylateHCID 86647449—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylateHCID 8668524153%

Reaction Steps

A solution of (9H-fluoren-9-yl)methyl 4-(diazoacetyl)piperidine-1-carboxylate (5 g, 13.3 mmol) in THF was cooled in an ice water bath and was treated with an aqueous HBr solution (10 mL). This reaction mixture was stirred at RT for 2 h. The reaction mixture was diluted with water and the organic content was extracted using EtOAc, dried over Na2SO4, filtered and concentrated at reduced pressure. The crude product was chromatographed over silica gel eluting with a gradient (0-15% EtOAc:hexanes) to afford (9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylate (3 g, 53%) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-df99140cba08482bb3c56295135abb14
Source noteuspto-grants-2016_05