HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843294Generated: October 30, 2026
Hydrochloric Acid → HCID 22617105, compound
https://huagongshe.com/reaction/843294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl carbazate | HCID 80519 | — |
| Reactant | HCID 13676208 | HCID 13676208 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22617105 | HCID 22617105 | — |
Reaction Steps
4.31 g (46.9 mmol) of methyl carbazate were initially charged in water (40 ml) and admixed with 4.75 g (46.9 mmol) of conc. hydrochloric acid (36% strength). 10.0 g (46.9 mmol) of diphenyl imidocarbonate (preparation of diphenyl imidocarbonate similar to the method of Heydayatullah, M. Bull Soc. Chim Fr. 1967, 416) were added a little at a time to this solution, at 7° C. After 4 hours of stirring with ice-bath cooling, the mixture was extracted with ethyl acetate (4×100 ml). The combined organic phases were dried over magnesium sulphate and, after filtration, concentrated under reduced pressure. The residue was dried under reduced pressure at 25° C. This gave 7.62 g of crude product containing phenol and methyl N′-diphenoxymethylenehydrazinecarboxylate in a ratio of 10:1. The yield of methyl N′-diphenoxymethylene-hydrazinecarboxylate was 693 mg (5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376699B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-2e09cec4a1a54c6eaddb6bc1bfe129f0 |
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| Source note | uspto-grants-2002_04 |
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