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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | Ethyl 3,3-diethoxypropionate | HCID 66389 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 3,4-dihydro-1H-2-benzopyran-1-acetate | HCID 10822798 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255090B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-c461eb3c2f084164a00c0ca805ef48d6 |
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| Source note | uspto-grants-2016_02 |
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