HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052583Generated: October 30, 2026
Ethylene Glycol → 6-Hydroxy-2,5,7,8-tetramethylchroman-2-acetic acid
https://huagongshe.com/reaction/2052583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Methylene-5-(2,4,5-trimethyl-3,6-diacetyloxy-phenyl)pentanenitrile | HCID 20333799 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Hydroxy-2,5,7,8-tetramethylchroman-2-acetic acid | HCID 5592 | 84% |
Reaction Steps
A mixture of 623 mg (1.89 mmoles) of the mixture of E- and Z-3-methyl-5-(2,4,5-trimethyl-3,6-diacetyloxyphenyl)-3-pentenenitrile and 3-methylene-5-(2,4,5-trimethyl-3,6-diacetyloxy-phenyl)pentanenitrile, 498 mg (7.70 mmoles) of 85% KOH, 5 ml of ethylene glycol and 0.5 ml of water was stirred and refluxed for 36 hr. The reaction mixture was cooled to room temperature, then poured into water. The pH of the solution was adjusted to 8 with 1 N aqueous HCl and the resulting mixture was extracted with two portions of ether (the extracts were discarded). The aqueous phase was acidified with 3 N aqueous HCl and worked-up with ether in the usual manner giving 421 mg (84%) of rac.-(6-hydroxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)acetic acid as a tan solid, mp 168°-170°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04186138 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-31ed43d0447b4f2aa231ff9fad9776cb |
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| Source note | uspto-grants-1980_01 |
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