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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774008Generated: October 31, 2026

Hydrochloric Acid → ethyl 3,4-dihydro-1H-2-benzopyran-1-acetate

https://huagongshe.com/reaction/1774008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-PhenylethanolHCID 6054—
ReactantEthyl 3,3-diethoxypropionateHCID 66389—
SolventDichloromethaneHCID 6344—
Productethyl 3,4-dihydro-1H-2-benzopyran-1-acetateHCID 10822798—

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice-cooled solution of phenethyl alcohol (1.21 mL, 10 mmol, 1.0 eq.) and ethyl 3,3-diethoxy-propionate (2.59 mL, 12 mmol, 1.2 eq) in DCM (5 mL), 1N titantetrachloride solution in DCM (22 mL, 22 mmol, 2.2 eq) was added dropwise. The mixture was stirred at 0° C. for 1 hour and further at r.t. for 3 hours. The mixture was poured onto ice and 2N aq. HCl soln. (30 mL). The layers were separated. The aq. phase was extracted with DCM (2×50 mL). The comb. org. phases were washed with sat. aq. NaCl soln. (1×50 mL), dried over Na2SO4, and concentrated in vacuo. The residue was purified by flashmaster (column: 100 g, flow: 45 mL/min, 40 fractions of 45 mL, Heptane to Heptane/AcOEt 85:15) to yield (±)-isochroman-1-yl-acetic acid ethyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255090B2
Source datasetuspto-grants-2016_02
ORD IDord-c461eb3c2f084164a00c0ca805ef48d6
Source noteuspto-grants-2016_02