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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856331Generated: October 29, 2026

Acetylene → 1-(4-Fluorophenoxy)but-3-yn-2-ol

https://huagongshe.com/reaction/1856331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(4-Fluorophenoxy)acetaldehydeHCID 11051869—
ReactantHCID 178418265HCID 178418265—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Fluorophenoxy)but-3-yn-2-olHCID 1278621648%

Reaction Steps

Acetylene gas, dried by passing through a trap containing sulfuric acid, is bubbled at a moderate rate, through 5 ml of vigorously stirred tetrahydrofuran, for 15 minutes. To this acetylenic solution, is then added dropwise, with continued passage of acetylene, 3.5 ml of a 2.4 M solution of n-butylmagnesium chloride in tetrahydrofuran (8.4 mmoles) over 45 minutes. The mixture is stirred a further 15 minutes, and a solution of 580 mg (3.9 mmoles) of p-fluorophenoxy acetaldehyde (Example 156) in 3 ml of tetrahydrofuran is added dropwise over 15 minutes. This solution is stirred for 2 more hours, with passage of acetylene, poured into 50 ml of a saturated solution of ammonium chloride, extracted twice with 50 ml of ether, washed with 10 ml of ammonium chloride solution, dried with magnesium sulfate, filtered, and evaporated. The crude subject product is purified by sublimation at 75° C. (0.1 mm) for 5 hours to give 330 mg (48%) of white crystals, mp 46°-47° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04218566
Source datasetuspto-grants-1980_08
ORD IDord-ddda18095105451f8cf205bbbd8f9b6c
Source noteuspto-grants-1980_08