HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395683Generated: October 26, 2026
Diethyl Ether → Ethyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate
https://huagongshe.com/reaction/1395683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 5-(4-acetylphenyl)benzofuran-2-carboxylate | HCID 20329647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate | HCID 20337913 | — |
Reaction Steps
1.2 g of sodium borohydride was added in one portion to a stirred mixture of 15.0 g of 6A, 200 ml of ether and 40 ml of ethanol. The mixture was stirred at room temperature for 2 hours. The solvents were evaporated under reduced pressure. 1.6 liters of water was added to the residue and the mixture was extracted with chloroform. The extract was dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was dissolved in 150 ml of chloroform. The solution was filtered through charcoal. 400 ml of hexane was added. The solid which formed was collected, recrystallized from a 3/50 v/v mixture of chloroform and hexane and dried in a vacuum oven to give ethyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate (6B), mp: 108°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04205080 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-f2806e7ba71e403b839e4f450a74392b |
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| Source note | uspto-grants-1980_05 |
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