HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 2,2-Dimethoxy-1-methylpropylcyanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 1-Methyl-2,2-dimethoxypropylamine | HCID 15851826 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2-Dimethoxy-1-methylpropylcyanamide | HCID 20164479 | — |
Reaction Steps
Cyanogen bromide (424 mg., 4 m moles) was added to a solution of 2,2-dimethoxy-1-methylpropylamine (266 mg., 2 m moles) and KHCO3 (400 mg., 4 m moles) in a mixture of water (2 ml.) and methanol (4 ml.). After 15 minutes the mixture was poured in to water (150 ml.) and the mixture extracted with CH2Cl2. The extract was washed with water and brine, dried (MgSO4) and evaporated to dryness to give 2,2-dimethoxy-1-methylpropylcyanamide as a pale yellow oil (280 mg., 88%) having the following n.m.r. spectrum in CDCl3 : 1.15 (s, 3H); 1.18 (d, 3H); 3.15 (s, 6H); 3.0-3.6 (m, 1H); 4.0 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04701556 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-e9d0f8d715f147ec9120a29ad7753af1 |
| Source note | uspto-grants-1987_10 |