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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493780Generated: October 30, 2026

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

https://huagongshe.com/reaction/1493780

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 89) 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 numberUS05023341
Source datasetuspto-grants-1991_06
ORD IDord-e2c0e686b58c4ab6b568708958db3da3
Source noteuspto-grants-1991_06