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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227520Generated: October 26, 2026

Benzyl chloroformate → 1-Benzyloxycarbonyl-5-chloro-3-formylindol

https://huagongshe.com/reaction/2227520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium hydrideHCID 24758—
Reactant5-chloro-1H-indole-3-carbaldehydeHCID 2795374—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyloxycarbonyl-5-chloro-3-formylindolHCID 18473987—

Reaction Steps

To a solution of 5-chloro-3-formylindole (5.00 g) in tetrahydrofuran (135 ml) was added sodium hydride (60% oil suspension, 3.53 g). The mixture was stirred for 20 minutes at room temperature. Carbobenzoxychloride (6.64 ml) was added to the mixture. After being stirred for 1 hour at room temperature, the whole was poured into ice water. The mixture was extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate. The solution was concentrated to give a residue, which was subjected to silica gel chromatography. Elution with hexane-ethyl acetate (5:1) provided 1-benzyloxycarbonyl-5-chloro-3-formylindol (5.74 g) as a crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414003B1
Source datasetuspto-grants-2002_07
ORD IDord-8f5c9c6849e442b09051d7787c265e50
Source noteuspto-grants-2002_07