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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067999Generated: November 4, 2026

Hydrochloric Acid → (4-Hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2067999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiazole-4-carboxaldehydeHCID 2763214—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium HypochloriteHCID 23665760—
Reactant2-(tert-butoxycarbonylamino)-4-(N-methoxy-N-methyl-aminomethyl)-5-fluorothiazoleHCID 58055049—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4-Hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl esterHCID 8664735045%

Reaction Steps

A solution of Intermediate 104: {5-Fluoro-4-[(methoxy-methyl-amino)-methyl]-thiazol-2-yl}-carbamic acid tert-butyl ester (7.5 g, 25.7 mmol) in THF (45 mL) and water (4.5 mL) was rapidly stirred and treated slowly dropwise with 6.15% sodium hypochlorite solution in water (Clorox™, 67 mL, 55 mmol). The resulting thiazole-4-carboxaldehyde was reduced in situ with sodium borohydride (0.5 g). The reaction was acidified with 2 N HCl (10 mL) and extracted with diethyl ether (2×50 mL). The extracts were dried with sodium sulfate and evaporated to leave an orange resin which purified by silica gel chromatography (80% EtOAc/hexane) to afford (4-hydroxymethyl-5-fluoro-thiazol-2-yl)-carbamic acid tert-butyl ester as a yellow foam (2.9 g, 45% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293919B2
Source datasetuspto-grants-2012_10
ORD IDord-56ce5b0f06204018890156781e93cacd
Source noteuspto-grants-2012_10