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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488593Generated: October 29, 2026

Thiourea → HCID 22270379, compound

https://huagongshe.com/reaction/488593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantHCID 22270723HCID 22270723—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 22270379HCID 22270379—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N-[2,3-bis(4-chlorophenyl)-1,1-dimethylpropyl]chloroacetamide (Step C, 1.3 g, 3.8 mmol) in ethanol (10 mL) and acetic acid (2 mL) was added thiourea (0.34 g, 4.5 mmol). The reaction was stirred at 80° C. overnight to give a white precipitate. The precipitate was removed by filtration and washed with ethanol (10 mL), and the filtrate was diluted with dilute aqueous sodium hydroxide and extracted with hexane (2×50 mL). The combined extracts were dried over sodium hydroxide, filtered, and concentrated to dryness, and the residue was taken up by hydrogen chloride in dioxane (4 M, 5 mL) and concentrated to dryness to give the title compound. 1H NMR (500 MHz, CD3OD): (free amine) δ 7.22-7.14 (m, 4H), 7.06 (d, 2H), 6.96 (d, 2H), 3.22 (dd, 1H), 2.95 (dd, 1H), 2.86 (dd, 1H), 1.16 (s, 3H), 1.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972295B2
Source datasetuspto-grants-2005_12
ORD IDord-3dac4017265e4bcf8fb431f9bacfebba
Source noteuspto-grants-2005_12