HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Ethyl 4-(4-hydroxy-3-oxobutyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-(3-oxopropyl)benzoate | HCID 2757377 | — |
| Reactant | Ethyl benzothiazolium bromide | HCID 68772949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(4-hydroxy-3-oxobutyl)benzoate | HCID 10609833 | — |
Reaction Steps
A mixture of 1.1 g (5 mmol) of 3-(4-carbethoxyphenyl)propanal and 150 mg (5 mmol) of paraformaldehyde in 10 mL of ethanol, together with 230 mg (0.9 mmol) of ethyl benzothiazolium bromide and 90 mg (0.9 mmol) of triethylamine, is heated at about 70° C. for 16 hours. The reaction mixture is concentrated in vacuo and the product further purified by chromatography on silica gel, eluting with 15:85 ethyl acetate:hexane, to yield ethyl 4-(4-hydroxy-3-oxobutyl)benzoate as a colorless oil which solidifies upon standing; m.p. 51°-52° C. Anal. calcd for C13H16O4 : C, 66.09; H 6.83. Found: C, 66.29; H, 6.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254687 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-b84a1bc7fcda459b8fc671faf878f9be |
| Source note | uspto-grants-1993_10 |