HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973183Generated: October 30, 2026
Dimethylamine → Thiourea, N'-(3-hydroxyphenyl)-N,N-dimethyl-
https://huagongshe.com/reaction/1973183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 3-isothiocyanatophenol | HCID 820026 | — |
| Reactant | Tert-butylcarbamate | HCID 21252905 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Thiourea, N'-(3-hydroxyphenyl)-N,N-dimethyl- | HCID 5368133 | — |
| Product | Tert-butylcarbamate | HCID 21252905 | — |
Reaction Steps
1-(meta-hydroxyphenyl)-3,3-dimethyl-2-thiourea, tert-butylcarbamate is prepared by charging to a suitable vessel about 25 g. (approximately 0.1 mole) meta-hydroxyphenyl isothiocyanate, tert-butylcarbamate dissolved in about 150 ml. of methanol, and adding, with stirring about 15.4 g. (approximately 0.12 moles) of 40 percent aqueous dimethylamine mixed with about 50 ml. of methanol in a single increment. The mass quickly solidifies as the temperature rises from about room temperature to about 60° C. The mass is cooled to about 15° C., separated from the residual liquid by filtration, washed with four 150 ml. portions of a 75 percent methanol/25 percent water solution and dried under vacuum overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996275 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-65de4daf46fe466b932d27eefec1abc3 |
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| Source note | uspto-grants-1976_12 |
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