Dimethylcarbamoyl Chloride → HCID 86098753, compound

Dimethylcarbamyl chloride (6.86 g, 63.7 mmol) was added slowly to 10.0 g (63.7 mmol) of N-octyl acetamide in 10 mL of dry toluene and the solution was refluxed under a nitrogen atmosphere for 16 h. The volatile materials were removed on a rotary evaporator in vacuo. The residue, dissolved 30 mL of dichloromethane, was stirred vigorously with a solution of 2.55 g (63.7 mmol) of sodium hydroxide in 40 mL of water for 30 min. Calcium carbonate (2.55 g) was added to the mixture and stirring was continued for an additional 30 min. The organic phase was separated and the aqueous phase was extracted with dichloromethane (30 mL×3). The combined organic phases were dried (calcium carbonate) and the solvent was removed on a rotary evaporator. The residue was distilled at 63-64° C./0.25 Torr to yield 6.2 g (53%) of product (purity 99% by GC). IR 2956, 2925, 2854 (C—H), 1626 (N═C) cm−1. 1H NMR 3.17 (t, 2H, JHH 7.5 Hz, —CH2—N═), 2.86 (s, 6H, —N—(CH3)2); 1.87 (s, 3H, —N═C(CH3)—N); 1.5 (m, 2H, —CH2—CH2—N═); 1.25-1.4 (m, 10H, CH3—(CH2)5—); 0.88 (t, 3H, JHH 7.2 Hz, CH3).

1. temperaturethe solution was refluxed under a nitrogen atmosphere for 16 h
2. customThe volatile materials were removed on a rotary evaporator in vacuo
3. dissolutionThe residue, dissolved 30 mL of dichloromethane
4. customThe organic phase was separated
5. extractionthe aqueous phase was extracted with dichloromethane (30 mL×3)
6. dry with materialThe combined organic phases were dried (calcium carbonate)
7. customthe solvent was removed on a rotary evaporator
8. distillationThe residue was distilled at 63-64° C./0.25 Torr

ORD record

ord-5f69823e400c4c6caf499b0d489bc5d6

Source dataset

uspto-grants-2016_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09433895B2