Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobutyric acid | HCID 75809 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | Benzyl 4-bromobutanoate | HCID 3832489 | — |
Reaction Steps
4-bromobutyric acid (10.6 g, 60 mmole) was dissolved in thionyl chloride (20 mml), and the reaction was kept for 4 hr. The solution was evaporated and coevaporated. with toluene several times. The residue was redissolved in dichloromethane (120 ml), and then benzyl alcohol (4.14 ml, 40 mmole) was added. The solution was cooled down to −50° C. and triethylamine (10 ml, 72 mmole) was added. The reaction mixture was slowly warmed to room temperature. After 3 hr, the reaction mixture was poured into sodium bicarbonate aqueous solution and the organic phase was washed with water and dried, giving the titled product, 6.8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974802B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-22650d784fa84b8983a0fb69758e77b4 |
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| Source note | uspto-grants-2005_12 |
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