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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871546Generated: November 3, 2026

Diiodomethane → 4,4-Dimethyl-8-iodochroman

https://huagongshe.com/reaction/1871546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant4,4-DimethylchromanHCID 316763—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product4,4-Dimethyl-8-iodochromanHCID 22592649—

Reaction Conditions

Temperature-78 °C

Reaction Steps

2.00 g (12.3 mmol) of 4,4-dimethylchroman and 30 ml of ethyl ether are introduced into a three-necked flask under argon. 2.4 ml (15.9 mmol) of tetramethylethylenediamine (TMEDA) are added dropwise, the mixture is cooled to -78° C. and 5.9 ml (14.8 mmol) of n-butyllithium (2.5M in hexane) are added dropwise. The temperature is allowed to return to -20° C. over two hours and then to room temperature and the mixture is stirred for 12 hours. 1.3 ml (16.0 mmol) of diiodomethane and 15 ml of ethyl ether are introduced into another three-necked flask under argon. Cooling is carried out to 0° C. and the preceding solution, cooled beforehand to -78° C., is introduced, then the reaction mixture is allowed to return to room temperature and stirred for 12 hours. The reaction mixture is poured into water and extracted with ethyl ether and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column eluted with heptane. After evaporating the solvents, 1.30 g (37%) of the expected compound are collected in the form of a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103762
Source datasetuspto-grants-2000_08
ORD IDord-9e21647454d74c8d98a54b97f0f9d845
Source noteuspto-grants-2000_08