Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13768688 | HCID 13768688 | — |
| Product | HCID 13768689 | HCID 13768689 | 48% |
Reaction Steps
To a stirred solution of 36 gm of concentrated H2SO4 at 5° C. was added 8.7 ml of acetic anhydride, and the mixture was stirred in the cold for about 0.5 hours. Acetonitrile (5.35 gm) was added, the solution was stirred for 5 minutes, and then 6.81 gm of N-methoxymethyl-2-chloro-N-[2-methyl-1-(1-methyl-ethyl)-1-propenyl]-acetamide was added. The reaction mixture was allowed to warm to room temperature over 4 hours and then partitioned between 100 ml of methylene chloride and 100 ml of H2O. The organic layer was washed with 75 ml of H2O, then 75 ml of saturated NaCl, and dried over MgSO4. Filtration and concentration gave an off-white solid which was washed through a 5 cm plug of silicagel with 50% ethyl acetate in hexane to afford 3.6 gm of product as a white solid (m.p. 113-114° C.). (48% yield) Analysis for C 12 H21ClN2O2 :
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665228 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-dd92566489e94078b4190bd1d3c3808f |
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| Source note | uspto-grants-1987_05 |
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