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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038757Generated: October 31, 2026

tert-Butanol → Tert-butyl (1-(5-iodopyridin-2-YL)cyclobutyl)carbamate

https://huagongshe.com/reaction/2038757

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(5-Iodopyridin-2-YL)cyclobutanecarboxylic acidHCID 67508444—
ProductTert-butyl (1-(5-iodopyridin-2-YL)cyclobutyl)carbamateHCID 6750927722.8%

Reaction Conditions

Temperature85 °C

Reaction Steps

1-(5-Iodo-pyridin-2-yl)-cyclobutane carboxylic acid (3.92 g, 12.9 mmol) was combined with tert-BuOH (6.1 mL, 65 mmol), Et3N (9.0 mL, 65 mmol) and DPPA (3.1 mL, 14 mmol). The reaction was heated to reflux (external bath: 85° C.) for 1.5 h. The volatiles were removed in vacuo and the crude reaction mixture was purified by normal phase flash chromatography on silica gel (5→80% EtOAc/hexanes) to give 1.1 g of [1-(5-iodo-pyridin-2-yl)-cyclobutyl]-carbamic acid tert-butyl ester as a solid, m/z 375.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575360B2
Source datasetuspto-grants-2013_11
ORD IDord-c546a4b2cd4b401f83ef17c80866eb45
Source noteuspto-grants-2013_11