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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416631Generated: October 30, 2026

Triphenylphosphine → (S)-Tert-butyl 2-(((5-bromopyridin-3-YL)oxy)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/1416631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Bromo-5-hydroxypyridineHCID 599529—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 131721282HCID 131721282—
SolventTetrahydrofuranHCID 8028—
Product(S)-Tert-butyl 2-(((5-bromopyridin-3-YL)oxy)methyl)azetidine-1-carboxylateHCID 10688713—

Reaction Steps

A 619.3 mg (3.31 mmol) sample of-1-BOC-2-(S)-azetidinemethanol, prepared as in Example 7b above, and 480 mg (2.76 mmol) of 5-bromo-3-hydroxypyridine, from Example 65b above, were reacted with triphenylphosphine and DEAD (3.31 mmol each) in 10 mL of THF according to the procedure of Example 14a, to give 887 mg of the title compound. MS (DCI/NH3) m/e 243/246 (M+H)+, 260/262 (M+NH4)+. 1H NMR (CDCl3, 300 MHz) δ: 8.35-8.25 (br, 2H), 7.44 (s, 1H), 4.55-4.47 (m, 1H), 4.39-4.29 (m, 1H), 4.16-4.10 (m, 1H), 3.98-3.85 (m, 2H), 2.42-2.33 (m, 2H), 1.42 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05914328
Source datasetuspto-grants-1999_06
ORD IDord-0bfe5cf078a0491985622422bc7bfd87
Source noteuspto-grants-1999_06