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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364014Generated: October 30, 2026

Tetrahydrofuran → HCID 66921872, compound

https://huagongshe.com/reaction/1364014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Acetoxyisobutyryl bromideHCID 2724715—
ReactantHCID 25019473HCID 25019473—
ProductHCID 66921872HCID 66921872—

Reaction Steps

To a stirred solution of diol 23 (7.42 g, 22.1 mmol) in THF (150 mL) at 0° C. under nitrogen atmosphere, α-acetoxyisobutyryl bromide (4.1 mL, 27.8 mmol) was added dropwise over a period of 10 min. The reaction mixture was stirred at same temperature for 30 min, and warmed to room temperature with stirring for 3.5 h. The solvent was evaporated, and the residual oil was partitioned between EtOAc (200 mL) and 5% aqueous NaHCO3 (50 mL). The organic layer was washed with water (100 mL), dried over MgSO4, filtered and concentrated to afford the crude bromoacetate 24 (9.05 g). The crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888337B2
Source datasetuspto-grants-2011_02
ORD IDord-e2e8382a46104cf7afb321f156115f6d
Source noteuspto-grants-2011_02