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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775871Generated: October 30, 2026

4-tert-Butylbenzoic acid → HCID 117740971, compound

https://huagongshe.com/reaction/1775871

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylbenzoic acidHCID 7403—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl α-amino-4-bromobenzeneacetateHCID 2764323—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
ProductHCID 117740971HCID 11774097188%

Reaction Steps

Prepared using General Procedure 7. To a stirring solution of methyl 2-amino-2-(4-bromophenyl)acetate (421 mg, 1.5 mmol), 4-(tert-butyl)benzoic acid (321 mg, 1.8 mmol), and DIEA (831 μl, 4.5 mmol) in DMF (3 mL) cooled to 0° C. was slowly added a solution of HATU (380 mg, 1.65 mmol) in DMF (1.5 mL) in a drop-wise fashion. The reaction mixture was allowed to warm slowly and stirring continued for 4 h. The reaction mixture was poured onto ice-water and the solid was filtered. The solid was dissolved in DCM (10 mL), dried over MgSO4 and evaporated to afford 532 mg (88%) of methyl 2-(4-bromophenyl)-2-(4-(tert-butyl)benzamido)acetate. LCMS-ESI (m/z) calculated for C20H22BrNO3: 403.0. found 404.1 [M+H]+, tR=3.61 min. (Method 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260427B2
Source datasetuspto-grants-2016_02
ORD IDord-9159f39f08a74649ad1c0e1e8356b24e
Source noteuspto-grants-2016_02