HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194935Generated: October 31, 2026
N,N-Dimethylaniline → HCID 88627764, compound
https://huagongshe.com/reaction/1194935
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 154041577 | HCID 154041577 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 88627764 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816452 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-508a622ce9164c52969fbc6272d9af67 |
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| Source note | uspto-grants-1989_03 |
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