Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | HCID 22910760 | HCID 22910760 | — |
| Product | HCID 22910763 | HCID 22910763 | 68% |
Reaction Steps
5-aminomethyl-3,3-dimethyl-2-methylene-1-tetradecyl-indoline (14.88 g, 38.75 mmol) was dissolved in methyl formate (75 ml) and heated to reflux (55° C.) under argon for 24 hours. The solution was then cooled to room temperature and the methyl formate evaporated. The residue was recrystallized from hexane to yield 5-(N-formylaminomethyl)-3,3dimethyl-2-methylene-1-tetradecyl-indoline (4) (10.85 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05667764 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-547a1fc34b3747ddb13965bed868c947 |
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| Source note | uspto-grants-1997_09 |
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