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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613369Generated: October 29, 2026

Hydrochloric Acid → Ethyl (+/-)-10,11 dihydro-3-methoxy-5H-dibenzo[a,d]cycloheptene-10-acetate

https://huagongshe.com/reaction/613369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl (+/-)-10,11-dihydro-10-hydroxy-3-methoxy-5H-dibenzo[a,d]cycloheptene-10-acetateHCID 18340682—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductEthyl (+/-)-10,11 dihydro-3-methoxy-5H-dibenzo[a,d]cycloheptene-10-acetateHCID 1546207091.3%

Reaction Steps

10% Pd/C (242 mg, 0.23 mmol) was added to a solution of ethyl (±)-10,11-dihydro-10-hydroxy-3-methoxy-5H-dibenzo [a,d]cycloheptene-10-acetate (741.1 mg, 2.27 mmol) and conc. HCl (0.19 mL, 2.27 mmol) in glacial AcOH (23 mL), and the mixture was shaken on a Parr apparatus at RT under H2 (50 psi). After 6 h, the reaction was filtered through celite®, and the filter pad was washed with EtOAc. The filtrate was concentrated, and the residue was reconcentrated from toluene. The resulting faintly yellow, oily residue was chromatographed (silica gel, 20% EtOAc/hexanes) to afford the title compound as a colorless oil (643.6 mg, 91%): TLC Rf 0.57 (20% EtOAc/hexanes); 1H NMR (250 MHz, CDCl3) δ 7.05-7.22 (m, 4H), 7.01 (d, J=8.2 Hz, 1H), 6.76 (d, J=2.7 Hz, 1H), 6.67 (dd, J=8.2, 2.7 Hz, 1H), 4.30 (d, J=15.0 Hz, 1H), 4.11-4.25 (m, 2H), 3.85 (d, J=15.0 Hz, 1H), 3.70-3.90 (m, 1H), 3.77 (s, 3H), 3.31 (dd, J=15.0, 4.1 Hz, 1H), 2.93 (dd, J=15.0, 9.2 Hz, 1H), 2.64 (dd, J=15.6, 5.0 Hz, 1H), 2.52 (dd, J=15.6, 9.3 Hz, 1H), 1.27 (t, J=7.1 Hz, 3H); FTIR (CCl4) 1734, 1611, 1504,1285, 1263, 1155, 1044 cm-1 ; MS (ES) m/e 333.0 (M+Na)+, 328.0 (M+NH4)+, 311.0 (M+H)+, 265.0 (M+H-EtOH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008213
Source datasetuspto-grants-1999_12
ORD IDord-7e28827a9a094ad58ca40892acd68b86
Source noteuspto-grants-1999_12