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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858765Generated: October 31, 2026

Hydrochloric Acid → HCID 22127919, compound

https://huagongshe.com/reaction/1858765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 54557925HCID 54557925—
SolventMethanolHCID 887—
SolventHCID 86755338HCID 86755338—
ProductHCID 22127919HCID 22127919—

Reaction Steps

From 2-trimethylsilylethyl (3RS,4RS)-4-(4-fluorophenyl)-3-[4-[3-(2-trimethylsilyl-ethoxymethoxy)-benzyloxy]-naphthalen-2-ylmethoxy]-piperidine-1-carboxylate there was obtained in analogy to the procedure described in Example 1(e) by cleavage of the 2-trimethylsilylethyl carbamate with tetrabutyl-ammonium fluoride in tetrahydrofuran (3RS,4RS)-4-(4-fluorophenyl)-3-[4-[3-(2-trimethylsilyl-ethoxymethoxy)-benzyloxy]-naphthalen-2-ylmethoxy]-piperidine, MS: 588 (M+H)+, as a light yellow oil, from which by cleavage of the SEM group by means of a 2N solution of hydrogen chloride in methanol analogously to the procedure described in Example 5(g) there was obtained (3RS,4RS)-4-(4-fluorophenyl)-3-[4-[3-hydroxy-benzyloxy]-naphthalen-2-ylmethoxy]-piperidine as a colourless solid; MS: 458 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-05bf93bee46b4c7faf2692111bb6145b
Source noteuspto-grants-2000_11