HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173149Generated: October 29, 2026
Lithium diisopropylamide → HCID 86693000, compound
https://huagongshe.com/reaction/2173149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2,2,2-Trifluoro-N-methoxy-N-methylacetamide | HCID 2782382 | — |
| Reactant | HCID 44253972 | HCID 44253972 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86693000 | HCID 86693000 | — |
Reaction Steps
A solution of 4-bromo-N,N-diethyl-2-methylbenzamide (500 mg, 1.851 mmol) in Tetrahydrofuran (4.63 ml) was cooled to −78 C and treated with LDA (2.313 ml, 4.63 mmol) for 15 minutes before 2,2,2-trifluoro-N-methoxy-N-methylacetamide (320 mg, 2.036 mmol) in Tetrahydrofuran (4.63 ml) was added to the reaction mixture and allowed to warm to room temperature. The reaction was stirred overnight and then partitioned between 1N HCl (100 mL) and EtOAc (100 mL). The aqueous layer was further extracted with EtOAc (2×50 mL). The combined organic layers were washed with brine (150 mL), dried over magnesium sulfate, filtered and concentrated. Purification using MPLC (0-20% EtOAc/Hex) affords 4-bromo-N,N-diethyl-2-(trifluoroacetyl)benzamide. LC-MS (IE, m/z): 366 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-62fb2c407bcf485eae59db5b607f1c77 |
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| Source note | uspto-grants-2015_06 |
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