HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990708Generated: October 29, 2026
Methanimidamide, hydrochloride (1:1) → HCID 67397995, compound
https://huagongshe.com/reaction/1990708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| Reactant | HCID 67398277 | HCID 67398277 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 67397995 | HCID 67397995 | 82.4% |
Reaction Steps
A mixture of 3.60 g (11.73 mmol) of 1-(4-chlorophenyl)-6-(tetrahydro-2H-pyran-2-yloxy)hex-2-yn-1-one, prepared in stage 5.2., of 9.45 g (117 mmol) of formamidine hydrochloride and of 25 g (234 mmol) of sodium carbonate in suspension in 108 ml of acetonitrile and 0.1 ml of water is stirred at 40° C. for 5 hours. The mixture is subsequently taken up in 600 ml of water and 400 ml of a saturated aqueous sodium carbonate solution. The organic phase is separated by settling, washed with 200 ml of water and 200 ml of a saturated aqueous sodium chloride solution, dried over sodium sulphate and evaporated. The residue is purified by chromatography on silica gel, elution being carried out with a 70/30 mixture of n-hexane and of ethyl acetate, to produce 3.22 g (9.67 mmol) of product in the form of a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645757B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-4797da0c03d146029c313baaa1c13a03 |
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| Source note | uspto-grants-2010_01 |
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