Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | HCID 15346052 | HCID 15346052 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 15346053 | HCID 15346053 | 67.2% |
Reaction Steps
A mixture of 2-[(1,1-diethylethyl)oxy]-6-chlorobenzamide (1.00 g, 3.9 mmol) and tetrabutylammonium bisulfate (0.13 g, 0.4 mmol) in 50% aqueous sodium hydroxide (25 mL) and toluene (15 mL) was heated to 100° C. and n-propyl bromide (0.43 mL, 4.7 mmol) in toluene (10 mL) was added over 30 min. The reaction was heated for 1 h, was cooled and poured into water. The mixture was extracted with ether and the organic layers were washed with brine, dried (MgSO4) and concentrated to a white solid. The crude product was purified by radial chromatography to afford 0.78 g (67%) of N-propyl 2-[(1,1-diethylethyl)oxy]-6-chlorobenzamide as a white solid: mp 100°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482974 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-c876f758466c42739f9b1a6254d1947f |
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| Source note | uspto-grants-1996_01 |
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