Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556135Generated: October 31, 2026

Methanol → 3,6-Diethynyl-9-methyl-9H-carbazole

https://huagongshe.com/reaction/556135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59806152HCID 59806152—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3,6-Diethynyl-9-methyl-9H-carbazoleHCID 5980616281.5%

Reaction Steps

A mixed solution containing dist. THF and dist. MeOH (dist. THF/dist. MeOH=3/1: 4 mL) as well as dist. H2O (0.1 mL) were added to and dissolved into 3,6-bis(trimethylsilylethynyl)-9-methylcarbazole (173 mg, 0.46 mmol) obtained in Synthesis example 12. Then, NaOH (35 mg, 0.88 mmol) was added, and the resultant mixed solution was stirred under a nitrogen atmosphere at room temperature for 4 hours to obtain a reaction mixture. After that, the reaction mixture was diluted with CH2Cl2. Then, an organic layer was washed with dist. H2O and sat. NaCl, and was dried with MgSO4. The dried organic layer was filtered and concentrated to obtain a crude product. Subsequently, the obtained crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=5/1) to obtain 3,6-diethynyl-9-methylcarbazole (86 mg, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053588B2
Source datasetuspto-grants-2011_11
ORD IDord-04b639c9ef2642aebbdeabe36155f592
Source noteuspto-grants-2011_11