HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839719Generated: October 25, 2026
Hydrochloric Acid → 1,4-Bis(3-hydroxy-2,2-dimethylpropyl)benzene
https://huagongshe.com/reaction/839719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1,4-Bis(2-carbomethoxy-2-methylpropyl)benzene | HCID 21312576 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,4-Bis(3-hydroxy-2,2-dimethylpropyl)benzene | HCID 20510740 | 40.8% |
Reaction Steps
To 500 ml of dry tetrahydrofuran was added 11.4 g of lithium aluminum hydride and 60 g of 1,4-bis(2-carbomethoxy-2-methylpropyl)benzene. The mixture was stirred overnight at room temperature. To the thick reaction mixture was added 300 ml of ethyl acetate, 30 ml of saturated aqueous NH4Cl and 5 ml of concentrated HCl. The mixture was stirred and filtered. Solvent was evaporated from the filtrate and the residue was recrystallized from benzene to obtain 20 g of 1,4-bis(3-hydroxy-2,2-dimethylpropyl)benzene. The solid from the above filtration was slurried with 50 ml of H2O, 20 ml of concentrated HCl and 150 ml of benzene and heated at reflux for 1 hour. The benzene layer was then separated, dried over MgSO4 at 80° C, filtered hot and then cooled to precipitate an additional 10 g of 1,4-bis(3-hydroxy-2,2-dimethylpropyl)-benzene, mp 104°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04096341 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-222f280891f4422187de49ae8e812013 |
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| Source note | uspto-grants-1978_06 |
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