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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173149Generated: October 29, 2026

Lithium diisopropylamide → HCID 86693000, compound

https://huagongshe.com/reaction/2173149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
Reactant2,2,2-Trifluoro-N-methoxy-N-methylacetamideHCID 2782382—
ReactantHCID 44253972HCID 44253972—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86693000HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-62fb2c407bcf485eae59db5b607f1c77
Source noteuspto-grants-2015_06