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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901728Generated: November 2, 2026

Tetrabutylammonium Fluoride → 2-[5-(4-Methoxyphenoxymethyl)-2-oxooxazolidin-3-yl]propanol

https://huagongshe.com/reaction/1901728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant3-(2-t-Butyldimethylsilyloxy-1-methylethyl)-5-(4-methoxyphenoxymethyl)oxazolidin-2-oneHCID 21474740—
SolventTetrahydrofuranHCID 8028—
Product2-[5-(4-Methoxyphenoxymethyl)-2-oxooxazolidin-3-yl]propanolHCID 2147469996%

Reaction Steps

A procedure similar to that described in Preparation 5(b) was repeated, except that 1.26 g of 3-(2-t-butyldimethylsilyloxy-1-methylethyl)-5-(4-methoxyphenoxymethyl)oxazolidin-2-one (polar isomer), obtained as described in Preparation 76, 9.6 ml of tetrabutylammonium fluoride (26% w/v in tetrahydrofuran) and 10 ml of anhydrous tetrahydrofuran were used, to give 0.86 g of the title compound, melting at 62° C. to 67° C., from the polar diastereomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578620
Source datasetuspto-grants-1996_11
ORD IDord-0de4d9200d9b41e080d0087fd3b8e48f
Source noteuspto-grants-1996_11