Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoin | HCID 8400 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(Benzyloxy)butanoic acid | HCID 562201 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70215516 | HCID 70215516 | — |
Reaction Steps
1.5 g of 4-benzyloxybutanoic acid are dissolved in 10 ml of anhydrous toluene in a reactor under a nitrogen atmosphere. 1.45 ml of 98% oxalyl chloride (2.1 eq.) and 4 drops of dimethylformamide, in order to catalyze the reaction, are subsequently added. The reaction mixture is left to react at room temperature for 1 hour. The solution is concentrated to dryness under vacuum. The orange oil obtained is dissolved in dichloromethane and then introduced dropwise into a reactor, placed under a nitrogen atmosphere, comprising a solution of 1.18 g (0.7 eq.) of benzoin and 1.58 g (2 eq.) of triethylamine in dichloromethane. An immediate evolution of gas is recorded. The reaction mixture is left stirring for 3 hours at room temperature. The reaction mixture is washed 3 times with water, dried over anhydrous sodium sulphate, filtered and finally brought to dryness. The esterified product is then isolated on a silica column (elutent:dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06333414B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-10dc0401f50f49d5bd67886eebee1a0a |
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| Source note | uspto-grants-2001_12 |
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