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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221972Generated: October 29, 2026

Sodium Hydroxide → 2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octane-2-carboxylic acid

https://huagongshe.com/reaction/221972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-(4-bromophenyl)-3-(2-(chloromethyl)-1,3-dioxolan-2-yl)propanoateHCID 59161535—
SolventDimethylformamideHCID 6228—
Product2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octane-2-carboxylic acidHCID 59161515—

Reaction Steps

To a solution of ethyl 2-(4-bromophenyl)-3-[2-(chloromethyl)-1,3-dioxolan-2-yl]propanoate (1-3) (27 g, 71.5 mmol) cooled to −78° C. in DMF (200 mL) was added NaH (8.58 g, 214 mmol) and the reaction was allowed to slowly warm from −78° C. to rt. Once at rt, 1N NaOH (100 mL) was added and the reaction mixture was stirred over night. The crude reaction mixture was poured into saturated sodium bicarbonate and washed with chloroform. The aqueous layer was acidified with HCl, extracted with chloroform, dried over sodium sulfate filtered and concentrated. The crude residue was purified by column chromatography eluting with 1-50% EtOAc/Hexane. The appropriate fractions were concentrated and recrystallized from EtOAc/hexane to give 2-(4-bromophenyl)-5,8-dioxaspiro[3.4]octane-2-carboxylic acid (1-4) as a white solid. MS (M+H)+: 314.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207169B2
Source datasetuspto-grants-2012_06
ORD IDord-90ec1c63679341569c7e0360a3c59bf1
Source noteuspto-grants-2012_06