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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410048Generated: November 1, 2026

Hexylamine → HCID 24830401, compound

https://huagongshe.com/reaction/2410048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexylamineHCID 8102—
ReactantPropanedioyl dichlorideHCID 74269—
ReactantHexyl isocyanateHCID 75659—
ReactantEthyl isocyanatoacetateHCID 76283—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 24830401HCID 2483040145%

Reaction Steps

Hexyl isocyanate (728 uL, 5.0 mmoles) was added to a solution of n-hexylamine (660 uL, 5.0 mmoles) in dichloromethane (100 mL) and the mixture stirred for 1 hour. Malonyl dichloride (486 uL, 5.0 mmoles) was added and the mixture was heated to gentle reflux for 1 hour. The mixture was washed with 1 molar hydrochloric acid (×2), dried and evaporated. The residue was redissolved in dichloromethane (50 mL) and diisopropylethylamine (1.73 mL, 10 mmoles) and the mixture was treated with ethyl isocyanatoacetate (561 uL, 5.0 mmoles). After stirring overnight the mixture was washed with 1 molar hydrochloric acid, dried and evaporated. The residue was dissolved in ethanol (5 mL) and treated with 6 molar sodium hydroxide (2.0 mL). The mixture was stirred for 1 hour, acidified and extracted into ethyl acetate. The organic solution was washed with 1 molar hydrochloric acid, dried and evaporated. The crude product was slurried in hexane to afford the title compound (890 mg, 45%). 1H NMR (400 MHz, DMSO-d6) δ ppm 13.10 (br. s, 1 H), 10.10 (t, J=4.80 Hz, 1 H), 4.13 (d, J=5.81 Hz, 2 H), 3.75-3.84 (m, 4 H), 1.53 (s, 4 H), 1.26 (s, 12 H), 0.82-0.90 (m, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815884B2
Source datasetuspto-grants-2014_08
ORD IDord-646faacada544b6e91c4aaa0e9216e0c
Source noteuspto-grants-2014_08