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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720127Generated: October 30, 2026

Prop-1-yn-1-amine → HCID 19033955, compound

https://huagongshe.com/reaction/1720127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProp-1-yn-1-amineHCID 17140—
ReactantNonanoyl chlorideHCID 69819—
SolventTriethylamineHCID 8471—
ProductHCID 19033955HCID 1903395562%

Reaction Steps

Propynylamine (10.4 ml, 151.2 mmol) was mixed with 150 ml of triethylamine in a round bottom flask immersed in a cold water bath, and vigorously stirred while nonanoyl chloride (27.0 ml, 149.75 retool) was added in portions from a dropping funnel over a 30 minute period. Additional triethylamine (100 ml) was added to facilitate stirring. At the end of the addition, the water bath was removed and the reaction was stirred for 30 minutes, then filtered. The filtrate was stripped down to a yellow solid. The solid was partitioned between ether and aqueous NaOH, requiring a considerable quantity of ether to dissolve. The combined ether extracts were stripped and recrystallized from heptane to give product as a white crystalline solid, 18.12 g, 92.8 mmol, 62% yield; top. 78°-79.5° C.; 1H NMR (CDCl3) ∂0.88 (t, J=6.0 Hz, 3 H), 1.28 (m, 10 H), 1.63 (m, 2 H), 2.19 (t, J= 7.6 Hz, 2 H), 2.22 (t, J=2.7 Hz, 1 H), 4.06 (dd, J=5.2, 2.6 Hz), 5.62 (br s, 1 H); EI mass spectrum m/z 196 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504237
Source datasetuspto-grants-1996_04
ORD IDord-e040a745165b4eac9bcfc6f59f02f34c
Source noteuspto-grants-1996_04