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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706621Generated: October 30, 2026

Hydrochloric Acid → 6-Hydroxy-2,5,7,8-tetramethylchroman-2-acetic acid

https://huagongshe.com/reaction/1706621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Methylene-5-(2,4,5-trimethyl-3,6-diacetyloxy-phenyl)pentanenitrileHCID 20333799—
ReactantZ-3-methyl-5-(2,4,5-trimethyl-3,6-diacetyloxyphenyl)-3-pentenenitrileHCID 20333801—
SolventEthylene GlycolHCID 174—
Product6-Hydroxy-2,5,7,8-tetramethylchroman-2-acetic acidHCID 559284%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208333
Source datasetuspto-grants-1980_06
ORD IDord-801e850c3db04c1baef84f7881e9984f
Source noteuspto-grants-1980_06