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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404843Generated: October 27, 2026

Potassium Carbonate → Tert-butyl 2-(3-hydroxypropoxy)ethoxy(methyl)carbamate

https://huagongshe.com/reaction/1404843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloroethoxy)ethanolHCID 12361—
Reactanttert-Butyl hydroxy(methyl)carbamateHCID 272414—
CatalystLithium BromideHCID 82050—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-(3-hydroxypropoxy)ethoxy(methyl)carbamateHCID 8662834372%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of N-Boc-N-methyl hydroxylamine (132 mg, 0.898 mmol), 2-(2-chloroethoxy)ethanol (168 mg, 1.35 mmol), K2CO3 (372 mg, 2.69 mmol) and LiBr (2 mg, 0.018 mmol) in DMF (3 mL) was heated at 100° C. and stirred for 16 h. The resulting mixture was cooled down to room temperature and filtered. The filtrate was concentrated and the residue was purified by silica gel flash column chromatography using 50% EtOAc/hexanes as eluent to afford the desired product as colorless oil (152 mg, 0.647 mmol, 72%). 1H NMR (CDCl3, 400 MHz): 8 (ppm) 1.45 (s, 9H), 2.68 (br s, 1H), 3.08 (s, 3H), 3.57-3.60 (m, 2H), 3.66-3.72 (m, 4H), 3.96-3.99 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916169B2
Source datasetuspto-grants-2014_12
ORD IDord-7d51bafebcfd4a5bbe14607258511b1b
Source noteuspto-grants-2014_12