Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081365Generated: October 31, 2026

Hydrochloric Acid → 2,2,4,4,7-Pentamethyl-6-acetylchroman

https://huagongshe.com/reaction/2081365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2,2,4,4,7-Pentamethyl-chromanHCID 15661124—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventNitromethaneHCID 6375—
Product2,2,4,4,7-Pentamethyl-6-acetylchromanHCID 15661137—

Reaction Steps

To an ice-bath cooled solution of 1.96 g (9.6 mmol) of 2,2,4,4,7-pentamethyl-chroman (Compound 46) in 30 ml of nitromethane was added under argon 1.059 g (13.5 mmol) of acetyl chloride followed by 1.9 g (14.3 mmol) of aluminum chloride. The reaction mixture was stirred at room temperature for 14 h and then cooled in an ice-bath and treated with 25 ml of conc. HCl. The mixture was warmed to room temperature and diluted with ether and water. The organic layer was separated and the aqueous layer extracted with ether. The organic extracts were combined and washed successively with water, saturated NaHCO3 solution, water again, and saturated NaCl solution, and then dried (MgSO4). The solvent was removed in vacuo and the residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as a pale yellow oil. PMR (CDCl3): & 1.36 (6H, s), 1.37 (6H, s), 1.86 (2H, s), 2.49 (3H, s), 2.56 (3H, s), 6.65 (1H, s), 7.74 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183827
Source datasetuspto-grants-1993_02
ORD IDord-2a4afb5e369e4b66bd007dd2cc5cd0dd
Source noteuspto-grants-1993_02