Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86649841 | HCID 86649841 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86649840 | HCID 86649840 | 99.1% |
Reaction Steps
Ethyl 54,54-dimethyl-4,12,20,28,36,44,52-heptaoxo-5,8,13,16,21,24,29,32,37,40,45,48,53-tridecaoxa-3,11,19,27,35,43,51-heptaazapentapentacontan-1-oate (Compound 13, 2.4 g, 0.0025 mol) was dissolved in THF (30 mL) and then stirred. After slowly adding 2 N lithium hydroxide aqueous solution (8 mL), the mixture was stirred at room temperature for 40 minutes. After removing THF from the reaction mixture, 1 N HCl aqueous solution was slowly added for acidification. After extracting 3 times with dichloromethane, the organic layer was separated, dried with magnesium sulfate, and then concentrated. The target compound 54,54-dimethyl-4,12,20,28,36,44,52-heptaoxo-5,8,13,16,21,24,29,32,37,40,45,48,53-tridecaoxa-3,11,19,27,35,43,51-heptaaza-1-pentapentacontanoic acid (Compound 14, 2.3 g, 99.1%) was yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450469B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-b94ff797237d43d0b53250dba7b69580 |
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| Source note | uspto-grants-2013_05 |
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