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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958477Generated: October 30, 2026

Isopropanol → Tert-butyl 5-bromothiazol-2-yl(isopropyl)carbamate

https://huagongshe.com/reaction/1958477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttert-butyl N-(5-bromo-1,3-thiazol-2-yl)carbamateHCID 21300388—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 5-bromothiazol-2-yl(isopropyl)carbamateHCID 5868835190.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 5-bromothiazol-2-ylcarbamate (3 g, 10.7 mmol), isopropanol (6.40 g, 107.4 mmol) and triphenylphosphine (5.63 g, 21.5 mmol) in THF (30 mL) was added diethyl azodicarboxylate dropwise at 0° C. The mixture was stirred at 0° C. and slowly warmed up to room temperature overnight. The solvent was evaporated. The residue was redissolved in dichloromethane (20 mL) and filtered to get rid of the undissolved solid. The filtrate was concentrated and purified by column chromatography on silica gel using 100% hexane to give a light yellow oil (3.10 g, 90% yield). LCMS (Conditions C): 4.19 min (RT); (M+H)+=267.01 (100%), 265.01 (95%), 224.95 (60%), 222.95 (60%). 1H NMR, 400 MHz, CDCl3: δ 7.34 (s, 1 H), 5.29 (m, 1 H), 1.59 (s, 9 H), 1.45 (d, 6.8 Hz, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410128B2
Source datasetuspto-grants-2013_04
ORD IDord-45af2ab1f3c94020a67123db43cec226
Source noteuspto-grants-2013_04