HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743887Generated: October 31, 2026
Acetyl chloride → Methanaminium, N-methyl-N-(phenylmethylene)-, chloride
https://huagongshe.com/reaction/1743887
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | N,N,N',N'-tetramethyl-1-phenylmethanediamine | HCID 584143 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methanaminium, N-methyl-N-(phenylmethylene)-, chloride | HCID 11073839 | 81% |
Reaction Steps
10 g (56 mmol) of N,N,N′,N′-tetramethyl-C-phenylmethanediamine (J. Am. Chem. Soc. 77,1955, p. 1114–1116) were dissolved in 100 ml of diethyl ether and cooled to 0° C. in an ice-bath. 4.0 ml (56 mmol) of acetyl chloride were added dropwise under nitrogen. After the first drops, a white salt was precipitated, the temperature rose slightly. After 15 hours at room temperature, the supernatant liquor was decanted off and the solid was washed three times with 100 ml of diethyl ether each time, filtered over a protective gas frit under nitrogen and dried under an oil-pump vacuum until a constant weight was reached. In that manner, 7.7 g of benzylidenedimethylammonium chloride (corresponding to 81% of the theoretically calculated yield) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012099B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-157f30fae4cc4a4b9cc73c468c1132f8 |
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| Source note | uspto-grants-2006_03 |
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