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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561776Generated: October 26, 2026

1-Propene, 3-methoxy- → Ethyl 3-(3-methoxypropyl)benzoate

https://huagongshe.com/reaction/561776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propene, 3-methoxy-HCID 69392—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantEthyl 3-bromobenzoateHCID 90488—
ReactantSodium MethoxideHCID 10942334—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(3-methoxypropyl)benzoateHCID 66761445—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a THF solution (0.1 M) of allyl methyl ether (1.4 eq.) was added, at 0° C., 9-borabicyclo[3.3.1]nonane (2.4 eq.) over a period of 30 min. The solution was stirred at 0° C. for 1 h and then warmed slowly to RT over 16 h. To the resulting clear solution was then added sodium methoxide (2.4 eq.), Cl2Pd(dppf)-dichloromethane complex (5% loading) and ethyl 3-bromobenzoate (1 eq.). The now brown suspension was heated to reflux for 16 h. The reaction mixture was cooled to RT, quenched with sat. aq. NH4Cl and extracted with ether. The combined organic extracts were washed with brine, dried over MgSO4 and filtered. Concentration of the filtrate in vacuo afforded a brown oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→4:1 (v/v) Hex:EtOAc) afforded the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063105B2
Source datasetuspto-grants-2011_11
ORD IDord-4adac288e2444c31ab9ac38dd0ab4339
Source noteuspto-grants-2011_11