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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640073Generated: November 1, 2026

Methanol → HCID 12862427, compound

https://huagongshe.com/reaction/1640073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantIsopropyl AcetateHCID 7915—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 45122633HCID 45122633—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 12862427HCID 1286242728.3%

Reaction Steps

7.18 g (189 mmol) of sodium borohydride was added to a solution of 10.76 g (65.5 mmol) of 4-methoxy-3H-benzofuran-2-one in 150 mL of ethyleneglycol dimethyl ether and stirred. While cooled on an ice-water bath, a solution of 5.25 mL (9.66 g, 94.5 mmol) of concentrated sulfuric acid in 21 mL of ethyleneglycol dimethyl ether was added dropwise thereto over 30 minutes. This mixture was heated and stirred on a 50° C. water bath for 49 minutes and then, while being stirred on an ice-water bath, 32 mL (25.3 g, 790 mmol) of methanol was added dropwise thereto for 6 minutes. This mixture was heated and stirred on a 50° C. water bath for 53 minutes, allowed to stand at room temperature overnight, 300 mL of isopropyl acetate and 200 mL of water were added therein and then the mixture was stirred for 5 minutes, transferred into a separatory funnel and settled. The aqueous layer was separated and discarded and after the organic layer was washed with 100 mL of water twice, the solvent was evaporated. The residue was crystallized from ethyl acetate-hexane and the obtained crystals were dried in vacuo at 30° C. and 3.12 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110688B2
Source datasetuspto-grants-2012_02
ORD IDord-08ce306f3cdf4607943d043bf0ee4c7e
Source noteuspto-grants-2012_02