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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916047Generated: October 31, 2026

Ammonium Chloride → 1-(2-Chloro-4-cyanophenyl)-4-(2,3-dihydrobenzofur-7-yl)-4-methyl-2-pentanol

https://huagongshe.com/reaction/916047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Chloro-p-toluonitrileHCID 88894—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3-(2,3-Dihydrobenzofur-7-yl)-3-methylbutanalHCID 58959939—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinoneHCID 22565281—
Product1-(2-Chloro-4-cyanophenyl)-4-(2,3-dihydrobenzofur-7-yl)-4-methyl-2-pentanolHCID 5896001766%

Reaction Steps

A solution of 2-chloro-4-cyanotoluene (606 mg) in THF/DMPU (1:1, 8 mL) was treated dropwise with LDA (1.8 M in heptane/ethylbenzene/THF, 2.44 mL) at −78° C. After 30 minutes, 3-(2,3-dihydrobenzofur-7-yl)-3-methylbutanal (400 mg) was added in THF (1 mL) and the mixture was subsequently warmed to room temperature. After 1 hour, 5 mL of saturated ammonium chloride solution was added. The organic phase was separated and the aqueous layer was extracted with 20 mL of ethyl acetate. The combined organic phases were washed with three 10 mL portions of water and dried over magnesium sulfate. The solvent was removed. Flash chromatography (hexanes-EtOAc (gradient from 10:1 to 5:1)) of the residue yielded 460 mg (66%) of 1-(2-chloro-4-cyanophenyl)-4-(2,3-dihydrobenzofur-7-yl)-4-methyl-2-pentanol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268152B2
Source datasetuspto-grants-2007_09
ORD IDord-a21f9c193894482aaa117c6a31fdbcdb
Source noteuspto-grants-2007_09