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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292481Generated: November 2, 2026

Carbon Dioxide → HCID 11805831, compound

https://huagongshe.com/reaction/2292481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant5-Bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furanHCID 10779312—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11805831HCID 11805831—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 5-bromo-7-tert-butyl-3,3-dimethyl-2,3-dihydrobenzo[b]furan (12.4 g, 44.0 mmol) in freshly distilled THF (44 mL) is cooled to -78° C. under Ar, and a solution of n-butyl lithium (2.5M in hexane; 15.0 mL, 37.5 mmol) is added dropwise via syringe. A slight exotherm is apparent, and a milky suspension results. The suspension is allowed to warm to -20° C., and then is cooled to -50° C. To the resulting suspension is added a large excess of freshly pulverized solid CO2. The resulting mixture is allowed to warm to 0° C. After 1 h, the mixture is partitioned between 0.1N NaOH (40 mL) and hexane (3×30 mL). The hexane layer is dried (MgSO4), filtered and evaporated to yield 7-tert-butyl-3,3-dimethyl-2,3-dihydrobenzo[b]furan. The aqueous layer is acidified to pH 2 with 1N HCl, and is extracted with Et2O (3×20 mL). The Et2O layers are combined, dried (MgSO4), filtered and evaporated to provide the desired carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684002
Source datasetuspto-grants-1997_11
ORD IDord-56a0ff67cac845dea5ebc928413d3cf7
Source noteuspto-grants-1997_11