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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901173Generated: October 31, 2026

Tetrabutylammonium Fluoride → 2-[2-(4-Methoxycarbonylmethylphenoxy)-1(S)-methylethyl]amino-1(S)-phenylethanol

https://huagongshe.com/reaction/1901173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantN-[2-(4-Methoxycarbonylmethylphenoxy)-1(S)-methylethyl]-2(S)-t-butyldimehylsilyloxy-2-phenylethanamineHCID 22867088—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(4-Methoxycarbonylmethylphenoxy)-1(S)-methylethyl]amino-1(S)-phenylethanolHCID 2286707979.7%

Reaction Steps

Following a procedure similar to that described in Example 27, but using 970 mg of N-[2-(4-methoxycarbonylmethylphenoxy)-1(S)-methylethyl]-2(S)-t-butyldimethylsilyloxy-2-phenylethanamine (prepared as described in Preparation 30), 20 ml of tetrahydrofuran and 1.7 g of tetrabutylammonium fluoride, 0.58 g of the title compound was obtained as crystals, melting at 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576340
Source datasetuspto-grants-1996_11
ORD IDord-78ad68c82363434fbb62fd7a88b4b1d2
Source noteuspto-grants-1996_11