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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338769Generated: October 29, 2026

tert-Butanol → tert-Butyl 3-iodobenzoate

https://huagongshe.com/reaction/338769

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant3-Iodobenzoic acidHCID 12060—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-iodobenzoateHCID 1838695992.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 3-iodobenzoic acid (50 g, 0.2 mol) in N,N-dimethylformamide (250 mL) was added solid 1,1′-carbonyldiimidazole (32.4 g, 0.2 mol) over 15 min. The resulting mixture was heated at 40° C. for 1 hr, then was added tert-butyl alcohol (29.6 g, 0.4 mol) and 1,8-diazabicyclo[5,4,0]undec-7-ene (30.4 g, 0.2 mol) and heated at 40° C. overnight. The reaction was cooled to room temperature, diluted with water (500 mL) and extracted with hexane (2×500 mL). The combined organic layers were washed with water (2×400 mL), brine (250 mL), dried over anhydrous magnesium sulfate (15 g), filtered and concentrated under reduced pressure to give the title compound (56 g, 92%) as an oil. NMR 60 MHz, (CDCl3), δ 8.3 (m, 1H), 7.8 (m, 2H), 7.0 (m, 1H), 1.6 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889870B2
Source datasetuspto-grants-2014_11
ORD IDord-7b0e1814b54a45b5bb283ceb1ab4f309
Source noteuspto-grants-2014_11