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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763162Generated: November 3, 2026

Triethylamine → HCID 178498348, compound

https://huagongshe.com/reaction/1763162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14013777HCID 14013777—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 178498348HCID 17849834832%

Reaction Steps

Product of Example 18 (23.34 g, 0.032 mol), 9.0 ml (0.064 mol) of triethylamine and 0.62 g of Pd/C (10% ) in 100 ml of EtOH were reacted as described by the preparation of product of Example 22 affording 9.99 g of dark orange oil. A portion of this oil (5.0 g, 0.014 mol), 4.51 g (0.070 mol) of 87% KOH, 1 ml of H2O in 30 ml of EtOH was stirred at reflux for 5 days. Reaction mixture was concentrated and the residue was poured into water and washed with ether. The aqueous layer was acidified with conc HCl, extracted with ether, dried (MgSO4) and concentrated in vacuo to 4.26 g of foamy oil. This oil was treated as described in Example 19: 4.26 g (0.013 mol) of this foamy oil, 25 ml of thionyl chloride and 25 ml of MeOH were reacted affording a dark solid residue which was taken up in ether and extracted with 15% K2CO3 and water, acidified with concentrated HCl, extracted with ether, dried (MgSO4) and concentrated in vacuo to 2.7 g of solid. Recrystallization from hexane-ether afforded 1.37 g (32.0%) of product as a tan solid: mp 83°-84.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835279
Source datasetuspto-grants-1989_05
ORD IDord-4d862c9fd7294d92b2065622164985b2
Source noteuspto-grants-1989_05