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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087652Generated: October 29, 2026

Formaldehyde → HCID 15181215, compound

https://huagongshe.com/reaction/1087652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDiisopropylamineHCID 7912—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Pentyn-1-olHCID 79346—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15181215HCID 1518121536%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of paraformaldehyde (7.14 g, 238 mmol), diisopropylamine (19.1 ml, 262 mmol) and cupric acetate monohydrate (1 g) in dioxane (40 ml) was heated in an oil bath of 60° C. for 1 hour. When the solid material disapeared, pent-4-yn-1-ol (20.02 g, 238 mmol) was added and the heating at 95° C. was continued until the greenish suspension had been completely replaced by a thin brown precipitate (approximately 3 hours). After cooling to 20° C., the reaction mixture was poured into 10% aqueous KOH (40 ml). The precipitate was filtered off and washed with ether (100 ml). The organic phase was washed with water (5 times 50 ml), dried (K2CO3) and evaporated to dryness to give the crude product. The isolated product was distilled to yield 16.88 g (36%) of 6-diisopropylaminohex-4-yn-1-ol: bp 116°-9° C. (0.05 mm Hg); 1H NMR (CDCl3) δ1.08(d, 12H), 1.40-1.98(m, 2H), 2.02-2.60(m, 2H), 2.83-3.44(m, 4H), 3.46-3.83(t, 2H), 4.09(s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036107
Source datasetuspto-grants-1991_07
ORD IDord-40d1a191d18244a8b1615444b4616ffd
Source noteuspto-grants-1991_07