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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709490Generated: October 29, 2026

Benzyl 4-Hydroxybenzoate → HCID 66865525, compound

https://huagongshe.com/reaction/709490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 2-bromo-2-methylpropionateHCID 90290—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66865525HCID 66865525—

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium hydride (0.664 g, 26.28 mmol) was added to a solution of 4-hydroxy-benzoic acid benzyl ester (5.0 g, 21.90 mmol) and 2-bromo-2-methyl-propionic acid tert-butyl ester (5.86 g, 26.28 mmol) in DMF (50 mL). The resulting mixture was warmed up to 80° C. and stirred for 1 h before additional 2-bromo-2-methyl-propionic acid tert-butyl ester (5.86 g, 26.28 mmol) and sodium hydride (0.664 g, 26.28 mmol) was added. After 18 h at 80° C. about 50% product could be detected by LC-MS. The reaction mixture was diluted with water and extracted with Et2O. The combined organic layers were dried (MgSO4) and evaporated and the desired product was isolated from the remaining mixture by HPLC. The title compound was obtained as an oil (2.5 g, 30.8%). 1H NMR (500 MHz, CDCl3): δ 7.96 (d, 2H), 7.43 (d, 2H), 7.37 (t, 2H), 7.33 (d, 1H), 6.82 (d, 2H), 5.32 (s, 2H), 1.60 (s, 6H), 1.40 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181181B2
Source datasetuspto-grants-2015_11
ORD IDord-59849cee3d124d5dab06312d605751f5
Source noteuspto-grants-2015_11