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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016476Generated: October 30, 2026

Triethylamine → 294622-57-4

https://huagongshe.com/reaction/1016476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThiophosgeneHCID 10040—
ReactantAmmonium HydroxideHCID 14923—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
SolventTetrahydrofuranHCID 8028—
Product294622-57-4HCID 1153596772.3%

Reaction Steps

A solution of ethyl 4-aminopiperidine-1-carboxylate (4.3 g, 0.025 mol) in dry THF was cooled to 0° C. and then treated with triethylamine (3.83 mL, 27.5 mol) and thiophosgene (2.1 mL, 27.5 mmol). The mixture was stirred for 1.5 hours at room temperature, cooled at 0° C. and then treated with ammonium hydroxide solution (7.7 mL, 28% in water). The mixture was stirred for approximately 12 hours and then concentrated by evaporation. The residue was taken up into ethyl acetate and the mixture was treated with a saturated solution of NaHCO3 and brine. The organic phase was separated, dried over sodium sulfate and then concentrated to dryness. The residue was taken up into diethyl ether and a resulting solid was collected by filtration and washed with diethyl ether to provide ethyl 4-thioureidopiperidine-1-carboxylate (4.18 g, 72% V). HNMR (dmso-d6): 7.57 (1H, d), 6.9 (1H, s), 4.05 (1H, bs), 4.02 (2H, q), 3.86 (2H, d), 2.89 (2H, bs), 1.82 (2H, bs), 1.20 (2H, m), 1.17 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476026B1
Source datasetuspto-grants-2002_11
ORD IDord-d0bbb9cbe1884ffdb4e57c04b282a185
Source noteuspto-grants-2002_11