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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487001Generated: November 3, 2026

9-Fluorenylmethyl chloroformate → HCID 71247928, compound

https://huagongshe.com/reaction/1487001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylateHCID 16228674—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71247928HCID 7124792890%

Reaction Steps

tert-Butyl 6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate (1 g, 1.0 eq.) was added to a solution of sodium bicarbonate (0.84 g, 2.0 eq.) in water (5 ml) at 5° C. FMOC—Cl (1.56 g, 1.2 eq.) in 1,4-dioxane (10 ml) was added dropwise. The reaction mixture was stirred at room temperature for 3 h, transferred into iced water (50 mL), and extracted with EtOAc (2×100 mL). The combined organic layers was washed with brine (2×50 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure (25° C., 20 mmHg) to afford 1.9 g of tert-butyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-azabicyclo[3.1.0]hexane-3-carboxylate (yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428490B2
Source datasetuspto-grants-2016_08
ORD IDord-67b942d6b8414d55a98c50c04cb1eb3e
Source noteuspto-grants-2016_08