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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191229Generated: November 2, 2026

(S)-tert-Butyl 2-(phenoxymethyl)pyrrolidine-1-carboxylate → (S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/2191229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-Butyl 2-(phenoxymethyl)pyrrolidine-1-carboxylateHCID 10636271—
Reactant(S)-tert-Butyl 2-((tosyloxy)methyl)azetidine-1-carboxylateHCID 11602568—
Product(S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylateHCID 1156517979%

Reaction Steps

(S)-tert-Butyl 2-(phenoxymethyl)azetidine-1-carboxylate (16) was prepared according to the same procedure for compound 9, except using compound 15, and purified with hexanes-ether (2:1) to afford 0.81 g (79%) of 16 as a colorless oil. 1H NMR (300 MHz, CDCl3) δ CDCl3 7.30 (m, 2H), 6.94 (m, 3H), 4.53 (m, 1H), 4.26 (m, 1H), 4.12 (m, 1H), 3.93 (m, 2H), 2.33 (m, 2H), 1.43 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329686B2
Source datasetuspto-grants-2012_12
ORD IDord-687d2629b79e49d895b356b5cee81d8f
Source noteuspto-grants-2012_12