Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Nonanoic acid, 9-hydroxy-, methyl ester | HCID 292983 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86597500 | HCID 86597500 | — |
Reaction Steps
To a mixture of oxalyl dichloride (18.85 ml) and dichloromethane (60 ml), dimethyl sulfoxide (2.99 ml) was added under a nitrogen atmosphere. The mixture was cooled in an ice-water bath and stirred therein for 15 minutes. 9-Hydroxynonanoic acid methyl ester (2.00 g) was added to the mixture. The mixture was stirred for 1 hour and triethylamine (10.8 ml) was added to the reaction mixture. The reaction mixture was stirred for 1 hour at ambient temperature and poured into a mixture of ethyl acetate (EA) and a saturated aqueous solution of ammonium chloride. The separated organic layer was washed with water and dried over magnesium sulfate. After filtration, the filtrate was concentrated in vacuo. The obtained residue was purified by chromatography on silica gel (eluted with 5% EA in n-hexane). The fractions including 8-formylnonanoic acid methyl ester were collected and concentrated in vacuo to give 8-formylnonanoic acid methyl ester (1.69 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468389B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-53c23a7f19c3409b91d5c63c45261018 |
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| Source note | uspto-grants-2008_12 |
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