HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693557Generated: November 1, 2026
Guanidine Hydrochloride → HCID 178524219, compound
https://huagongshe.com/reaction/1693557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-[3-(dimethylamino)acryloyl]benzoate | HCID 53416580 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178524219 | HCID 178524219 | — |
Reaction Steps
To a suspension of 4-(3-Dimethylamino-acryloyl)-benzoic acid methyl ester (1 g, 4.29 mmol; Prepared according to the method reported by S. Murahashi et al. Bulletin of the Chemical Society of Japan, 1987, 60, 3285) in MeOH (8.5 mL) is added guanidine hydrochloride (1.23 g, 12.86 mmol) and NaOH (412 mg, 10.3 mmol). The mixture is stirred at 80° C. for 24 h and then cooled down to room temperature. The mixture is concentrated and treated with H2SO4/H2O (1:1, 20 mL) and heated to 120° C. for 14 h. After cooling down to room temperature, the mixture is basified by pouring into ice cold NH4OH (50 mL) and acidified to pH= 1 by adding concentrated hydrogen chloride solution. The precipitate is collected by filtration, washed with acetonitrile and dried in a vacuum oven for 24 h to yield 680 mg of crude 4-(2-hydroxy-pyrimidin-4-yl)-benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158634B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-afabf17850b446c68100f4b3a9b965eb |
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| Source note | uspto-grants-2012_04 |
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