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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776281Generated: October 31, 2026

2-Methyl-3-butyn-2-ol → HCID 59354753, compound

https://huagongshe.com/reaction/1776281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
Reactant4-MethoxybenzaldehydeHCID 31244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59354753HCID 5935475378%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Too pre-cooled, −78° C. stirred solution of 2-methylbut-3-yn-2-ol (4.3 g, 0.04 mol) in dry THF (150 mL) n-BuLi (39.9 mL, 0.03 mol, 1.6 M in hexane) was added dropwise over 10 minutes under an inert atmosphere. The mixture was stirred for 30 min at −78° C., and then a solution of 4-methoxy-benzaldehyde (5 g, 0.037 mol) in dry THF (30 mL) was added to reaction mixture and stirring was continued for an additional 40 min at −78° C. The reaction mixture was then quenched with a saturated NH4Cl solution and extracted with EtOAc (2×100 mL). The combined organic layers were washed with water (100 mL) and brine (100 mL), dried over Na2SO4, filtered and concentrated in vacuo to obtain crude material. The crude material was purified via silica gel column chromatography eluting with 5% EtOAc in hexanes to afford 1-(4-methoxyphenyl)-4-methylpent-2-yne-1,4-diol (6.3 g, 78%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-b6e39f42802446228163300609c87c52
Source noteuspto-grants-2016_02