Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380390Generated: November 2, 2026

Methanesulfonic Acid → HCID 18955530, compound

https://huagongshe.com/reaction/2380390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 9951074HCID 9951074—
SolventO-XyleneHCID 7237—
ProductHCID 18955530HCID 1895553055%

Reaction Conditions

Temperature95 °C

Reaction Steps

2.41 g (20.0 mmol) of pivaloyl chloride are added dropwise over a period of 10 minutes to a suspension of 2.70 g (10.0 mmol) of 3-(4-ethoxyphenyl)-5-hydroxybenzofuran-2-one (compound (136), Table 1, Example 1) in 10 ml of xylene and 0.1 ml of methanesulfonic acid which is stirred at 95° C. under a nitrogen atmosphere. The clear, homogeneous reaction mixture is then refluxed for 2.5 hours and then concentrated under a slight vacuum. The residue is taken up in dichloromethane and washed with saturated sodium bicarbonate solution and water. The organic phases are combined, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. The residue gives 1.95 g (55%) of 3-(4-ethoxyphenyl)-5-pivaloyloxybenzofuran-2-one, oil (compound (135), Table 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05367008
Source datasetuspto-grants-1994_11
ORD IDord-f11057f217d245a48009c30b41a1dd82
Source noteuspto-grants-1994_11