Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020320Generated: October 26, 2026

3-Methylbenzaldehyde → HCID 58598880, compound

https://huagongshe.com/reaction/1020320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzaldehydeHCID 12105—
Reactant18-Crown-6HCID 28557—
ReactantEthyl 3-methylcinnamateHCID 589327—
Reactant5-Methoxy-6-chloro-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrroleHCID 11708502—
ReactantEthyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetateHCID 11759356—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58598880HCID 58598880—

Reaction Steps

3-m-Tolyl-acrylic acid ethyl ester. (Scheme 3) KHMDS (4.0 g, 20.0 mmol) was added to a solution of ethyl[bis(2,2,2-trifluoro-ethoxy)phosphinyl]acetate (4.7 mL, 20.0 mmol) and 18-crown-6 (10.6 g, 40.0 mmol) in THF (200 mL) at −78° C., and stirred for 30 minutes. m-Tolualdehyde (2.1 mL, 18 mmol) was added and the reaction mixture was stirred for 3 hours from −78° C. to room temperature. The reaction was quenched with aqueous hydrochloric acid (1M solution, 100 mL), and the product was extracted with EtOAc (3×100 mL). The organic extracts were washed with brine (100 mL), dried over MgSO4, and concentrated to afford the subtitle compound, which was used without further purification. MS calculated for C12H14O2+H: 191, observed: 191.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716324B2
Source datasetuspto-grants-2014_05
ORD IDord-df2956738c2140a4a8ce6177e911ca97
Source noteuspto-grants-2014_05