HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303448Generated: October 30, 2026
Hydrochloric Acid → Hexahydro-3H-benzofuran-2-one
https://huagongshe.com/reaction/2303448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Oxocyclohexylacetic acid | HCID 10920754 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Hexahydro-3H-benzofuran-2-one | HCID 95391 | — |
Reaction Steps
2-Oxocyclohexylacetic acid (31.2 g, 200 mmol) is dissolved in 125 ml of 0.2 N aqueous sodium hydroxide solution and, at room temperature, added dropwise to a solution of sodium borohydride (18.9 g, 500 mmol) in 150 ml of 0.2 N aqueous sodium hydroxide solution. The mixture is stirred for 20 h and then cooled to 0° C. and carefully acidified with 6 N HCl. The strongly acidic solution is then heated at 100° C. for 30 min and subsequently stirred overnight. The cold mixture is then extracted with MTBE, and the combined ether phases are washed with 5% strength sodium carbonate solution and sat. NaCl solution, dried over magnesium sulphate, filtered and concentrated. Purification is carried out by distillation (b.p.: 75° C./0.01 mm). Yield: 22.9 g (81.7%). MS (CI): m/e=141 [M+H+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06433004B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-4fc3c65af649429ea5b88d84146e879b |
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| Source note | uspto-grants-2002_08 |
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