Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194935Generated: October 31, 2026

N,N-Dimethylaniline → HCID 88627764, compound

https://huagongshe.com/reaction/1194935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantThioureaHCID 2723790—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 154041577HCID 154041577—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductHCID 88627764HCID 88627764—

Reaction Steps

Ethyl 4-bromo-(Z)-2-(cis 3-methylcyclohexyl)oxyimino-3-oxobutyrate (7.2 mmol) was treated with N,N-dimethylaniline (0.91 ml; 7.2 mmol) and thiourea (0.55 g, 7.2 mmol) in ethanol as described in Example 4d, except that the reaction was worked up after 2 h. The title compound was obtained as a white crystalline solid (1.78 g; 79%) m.p. 91°-93° C. (ethyl acetate/hexane), (Found: C, 54.29; H, 6.88; N, 13.57. C14H21N3O3S requires C, 54; H, 6.79; N, 13.49%), νmax (CHCl3) 3480, 3400, 1730, and 1610 cm-1 ; δH (CDCl3) 0.64-1.1 (2H, m, partially obscured by d, δ 0.92), 0.92 (3H, d, J 5.5 Hz), 1.1-1.55 (3H, m, partially obscured by t, δ 1.36), 1.36 (3H, t, J 7.1 Hz), 1.55-1.70 (1H, m) 1.70-1.86 (1H, m), 2.03-2.25 (2H, m), 4.20 (1H, tt, J 11.1 and 4.3 Hz), 4.39 (2H, q, J 7.1 Hz), 5.31 (2H, broad s), and 6.7 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816452
Source datasetuspto-grants-1989_03
ORD IDord-508a622ce9164c52969fbc6272d9af67
Source noteuspto-grants-1989_03