HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507014Generated: October 29, 2026
Benzyl Alcohol → 1-(Phenylmethyl) butanedioate
https://huagongshe.com/reaction/507014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Phenylmethyl) butanedioate | HCID 8788 | 70.5% |
Reaction Steps
A mixture of 5.0 g (0.05 mol) of succinic acid anhydride, 5.4 g (0.05 mol) of benzyl alcohol, 16.25 g (0.05 mol) of cesium carbonate, and 50 ml of N,N-dimethylforamide was stirred at 100° C. for 2 hours. The reaction mixture was cooled to room temperature, and then poured into 200 ml of ethyl acetate. The mixture was washed with saturated aqueous NaCl containing 0.35 N HCl (3×100 mL). The ethyl acetate phase, which contains the product, was collected and dried over anhydrous MgSO4. The MgSO4 was removed via filtration, and the ethyl acetate was removed under reduced pressure. The crude product was purified by crystallization in diethyl ether and hexane to provide 7.34 g of succinic acid monobenzyl ester, 70.47%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786134B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-f4d393c05f184f7fbd779904b5d5b30f |
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| Source note | uspto-grants-2010_08 |
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