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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988840Generated: October 31, 2026

Benzoic Acid → 6,8-Di-t-butyl-2-butoxycarbonylchroman

https://huagongshe.com/reaction/988840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantButyl AcrylateHCID 8846—
Reactant2,4-di-t-butyl-6-butoxymethyl-1-hydroxybenzeneHCID 9943927—
Solvent1-ButanolHCID 263—
Product6,8-Di-t-butyl-2-butoxycarbonylchromanHCID 1135996287%

Reaction Conditions

Temperature157.5 °C

Reaction Steps

Butyl acrylate (771.2 g, 6.02 mol) and benzoic acid (12.26 g, 0.10 mol) were added to 2,4-di-t-butyl-6-butoxymethyl-1-hydroxybenzene (665.2 g, net 586.71 g, 2.01 mol) obtained in Example 1, and the mixture was stirred while heating at 150-165° C. for 30 h. 1-Butanol produced by the reaction was removed. After the completion of the reaction, the reaction mixture was quantitatively analyzed by liquid chromatography according to the internal standard method. As a result, 6,8-di-t-butyl-2-butoxycarbonylchroman was obtained in a yield of 87% (1.74 mol). At this time, 6,8-di-t-butyl-3-butoxycarbonylchroman (a position isomer) was produced in about 8%. For use in the next step, excess butyl acrylate was distilled away under reduced pressure, toluene was added to the residue, and benzoic acid was removed with aqueous sodium hydrogen carbonate solution. The 1H-NMR data of the obtained 6,8-di-t-butyl-2-butoxycarbonylchroman are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635772B2
Source datasetuspto-grants-2003_10
ORD IDord-58ed17b60a5345f48a432d6639dd9ff0
Source noteuspto-grants-2003_10