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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588500Generated: October 26, 2026

2-Methyl-2-butene → 2-(1-{[(Tert-butoxy)carbonyl]amino}ethyl)-1,3-thiazole-5-carboxylic acid

https://huagongshe.com/reaction/588500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
ReactantTert-butyl 1-(5-formylthiazol-2-yl)ethylcarbamateHCID 86657335—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-(1-{[(Tert-butoxy)carbonyl]amino}ethyl)-1,3-thiazole-5-carboxylic acidHCID 6739600961.6%

Reaction Steps

A mixture of tert-butyl 1-(5-formylthiazol-2-yl)ethylcarbamate (3.5 g, 0.014 mol), sodium dihydrogen phosphate dihydrate (2.9 g, 0.019 mol) and 2-methyl-2-butene (3.85 g, 0.055 mol) in tert-butyl alcohol (70 ml) and water (40 mL) was stirred at room temperature for 30 minutes. Sodium chlorite (3.22 g, 0.035 mol) was added and the reaction maintained at room temperature for an additional 2 hours. The reaction was concentrated, diluted with water (50 mL) and acidified (pH=4) with the addition of 3N H3PO4. The mixture was extracted with DCM, the organic layer dried over anhydrous Na2SO4 and evaporated to dryness to afford 2-(1-(tert-butoxycarbonylamino)ethyl)thiazole-5-carboxylic acid (2.35 g, 60%). LC-MS: (FA) ES+ 273.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227951B2
Source datasetuspto-grants-2016_01
ORD IDord-70f31c8f91b149c1b20024a757314c11
Source noteuspto-grants-2016_01