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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18926Generated: October 25, 2026

Benzyl chloroformate → methyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/18926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylateHCID 18322367—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productmethyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylateHCID 68682038—

Reaction Steps

A mixture of the previously prepared methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate (0.400 g, 2.0 mmol) and NaH (60% w/w, 0.760 g, 4.5 mmol) in THF (4 mL) was stirred at room temperature for 30 min. To the resulting mixture was added benzyl carbonochloridate drop wise and stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution. The crude product was recrystallized from dichloromethane:hexane to afford the desired methyl 3-(benzyloxycarbonyl)-5-tert-butyl-1H-pyrrole-2-carboxylate (0.560 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741479B2
Source datasetuspto-grants-2010_06
ORD IDord-15201a1c4ea34fa8bc1c4db79bf5c082
Source noteuspto-grants-2010_06