HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride, 2-chloro-4-nitro- → tert-Butyl 2-chloro-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride, 2-chloro-4-nitro- | HCID 81522 | — |
| Reactant | 2-Propanol, 2-methyl-, lithium salt (1:1) | HCID 23664764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 2-chloro-4-nitrobenzoate | HCID 22593093 | 88% |
Reaction Steps
Lithium tert-butylate (2.2 M in tetrahydrofuran, 6.2 mL, 13.6 mmol) was added to a solution of 2-chloro-4-nitrobenzoyl chloride (2.00 g, 9.09 mmol) in tetrahydrofuran (12 mL) at 0° C. The orange solution was kept at 0° C. for 1.5 h, then allowed to reach room temperature over 16 h, then partitioned between 1 M aq. sodium carbonate solution and isopropyl acetate. The organic layer was dried (MgSO4) and evaporated to afford tert-butyl 2-chloro-4-nitro-benzoate (2.05 g, 88%) which was directly used in the next step. Brown oil, MS (EI)=257.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696200B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-5ba43986e0444cef8f15945ae2b2b5c5 |
| Source note | uspto-grants-2010_04 |