HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909899Generated: October 30, 2026
Methyl morpholine oxide → HCID 86654435, compound
https://huagongshe.com/reaction/1909899
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 67255556 | HCID 67255556 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86654435 | HCID 86654435 | 47.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598355B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e250af7649df42639e7d9b5de7d8657b |
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| Source note | uspto-grants-2013_12 |
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