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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818954Generated: November 2, 2026

Tetrahydrofuran → tert-butyl N-(5-formyl-1,3-thiazol-2-yl)carbamate

https://huagongshe.com/reaction/1818954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCornforth reagentHCID 2724130—
ReactantTert-butyl 5-(hydroxymethyl)thiazol-2-ylcarbamateHCID 53397352—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-(5-formyl-1,3-thiazol-2-yl)carbamateHCID 53393345—

Reaction Steps

To a solution of compound 62.2 (18.5 mmol) in dichloromethane is added molecular sieves (4.0 g) and PDC (39.0 mmol) at room temperature (THF is added to help dissolve the starting material). After 1.5 hours, an additional equivalent of PDC is added and the reaction is stirred for 5.5 hours. The reaction mixture is poured directly onto a silica gel column and is eluted with a gradient of 100% dichloromethane to 100% EtOAc. Fractions containing the desired product are pooled and concentrated to afford (5-formyl-thiazol-2-yl)-carbamic acid tert-butyl ester (compound 62.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601725B2
Source datasetuspto-grants-2009_10
ORD IDord-6c5cab683b3c441fbfc686c9d6fa5311
Source noteuspto-grants-2009_10