HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722626Generated: November 2, 2026
Dimethylhexadecylamine → HCID 70390925, compound
https://huagongshe.com/reaction/1722626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylhexadecylamine | HCID 16221 | — |
| Reactant | Benzene, 1-(chloromethyl)-3(or 4)-ethenyl- | HCID 11768772 | — |
| Catalyst | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Product | HCID 70390925 | HCID 70390925 | 75% |
Reaction Steps
In a 100 ml flask commercial vinylbenzyl chloride (3.05 g, 0.020 mol) was mixed with hexadecyldimethylamine (5.4 g, 0.020 mol) without any additional solvent. After addition of 2,6-di-tert-butyl-4-methylphenol (100 mg, 0.45 mmol) the mixture was heated overnight at 50° C. The solid product which formed was washed several times with dry ether, dried under vacuum at room temperature, and recrystallized from acetone/ether to give 6.3 g (75%) of 4-styrylmethyl (hexadecyl)dimethylammonium chloride. 1H NMR (CDCl3 /Me4Si): 0.88 (s, 3H), 1.24 (br s, 26H ), 1.78 (s, 2H), 3.30 (s, 6H), 3.53 (s, 2H), 5.08 (s, 2H), 5.32 (d, J=10.8 Hz, 1H), 5.84(d, J=18 Hz, 1H), 6.7 m, 1H), 7.51 (m, 4H). IR (KBr); 3020, 2920, 1640 cm-1. The critical micelle concentration (CMC) was 1.28× 10-2M at 25° C. determined conductometrically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857493 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-6b7c32855479448c82d25663395fb337 |
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| Source note | uspto-grants-1989_08 |
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