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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909899Generated: October 30, 2026

Methyl morpholine oxide → HCID 86654435, compound

https://huagongshe.com/reaction/1909899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 67255556HCID 67255556—
SolventAcetonitrileHCID 6342—
ProductHCID 86654435HCID 8665443547.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of tert-butyl 5-bromo-7-(bromomethyl)-6-chloro-1H-indole-1-carboxylic acid (7.2 g) and acetonitrile (50 mL) was added 4-methyl morpholine-4-oxide (2.7 g) at room temperature. The reaction mixture was stirred at 50° C. for 7 hours and then at 70° C. overnight. The reaction mixture was concentrated under reduced pressure, ethyl acetate and water were added thereto, and a liquid-separation operation was carried out. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0-90:10) to obtain tert-butyl 5-bromo-6-chloro-7-formyl 1H-indole-1-carboxylic acid (2.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-e250af7649df42639e7d9b5de7d8657b
Source noteuspto-grants-2013_12