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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179731Generated: October 31, 2026

1,4-Dioxane → (1R,3S)-3-[(tert-Butoxy)carbonyl]-2,2-dimethylcyclobutane-1-carboxylic acid

https://huagongshe.com/reaction/2179731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactanttert-butyl (1S,3R)-3-acetyl-2,2-dimethylcyclobutane-1-carboxylateHCID 21576610—
Product(1R,3S)-3-[(tert-Butoxy)carbonyl]-2,2-dimethylcyclobutane-1-carboxylic acidHCID 2157661178%

Reaction Steps

A stirred solution of (1S,3R)-tert-butyl 3-acetyl-2,2-dimethylcyclobutanecarboxylate (2.4 g, 10.62 mmol) in dioxane (270 ml) aqueous NaOBr solution (about 180 ml) was added slowly at about 0° C. and stirred at the same temperature for about 3 hours then allowed to stirred at room temperature for about 4 hours (the yellow colored solution turned to white color). After completion of the reaction (monitored by TLC), the reaction mixture was washed with methyl t-butyl ether (3×150 ml), the aqueous layer was adjusted pH (2-3) with 1N HCl and the aqueous layer was extracted with EtOAc and dried over Na2SO4 and the solvent was evaporated to afford title compound as an off white liquid. Wt: 1.9 g; Yield: 78%; 1H NMR (300 MHZ, CDCl3): δ 2.82-2.67 (m, 2H), 2.57-2.50 (m, 1H), 2.04-1.98 (m, 1H), 1.42 (s, 9H), 1.34 (s, 3H), 1.05 (s, 3H); IR (KBr, cm−1): 3205, 1731, 1694, 1460, 1371, 1236, 1157, 1108, 846, 721; Mass: [M+Na]+ 251 (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067966B2
Source datasetuspto-grants-2015_06
ORD IDord-e15d15d574074ea9ac266c67a5079182
Source noteuspto-grants-2015_06