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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270642Generated: October 25, 2026

Trimethyl borate → 2-(3-Hydroxymethylthiophen-2-yl)ethanol

https://huagongshe.com/reaction/270642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantLithium BromideHCID 82050—
ReactantMethyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylateHCID 58952963—
ReactantHCID 178418435HCID 178418435—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Hydroxymethylthiophen-2-yl)ethanolHCID 1118276190.6%

Reaction Steps

To 800 mL of anhydrous tetrahydrofuran, 31.0 g of sodium boron hydride and 71.3 g of lithium bromide were added, and then 10.6 mL of trimethyl borate was added thereto dropwise at 0° C. The resulting mixture was stirred at room temperature for 30 minutes, and then a solution obtained by dissolving 70.4 g of the compound obtained in Example 1 in 200 mL of tetrahydrofuran was slowly added over 2 hours while allowing the resulting mixture to reflux. The reaction solution was further refluxed for 2 hours then cooled to room temperature. 100 mL of anhydrous methanol was added slowly to the solution, and then 700 mL of ethyl ether and 700 mL of water were added. The organic phase was collected, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain 47.1 g (yield of 90%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449580B2
Source datasetuspto-grants-2008_11
ORD IDord-da60a17647834b40847d67500597ec76
Source noteuspto-grants-2008_11