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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909938Generated: October 30, 2026

1-Ethyl-1H-pyrazole-4-boronic acid, pinacol ester → tert-Butyl 3-(3-(1-ethyl-1H-pyrazol-4-yl)phenethoxy)propanoate

https://huagongshe.com/reaction/909938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-1H-pyrazole-4-boronic acid, pinacol esterHCID 11379045—
Reactanttert-Butyl 3-(3-bromophenethoxy)propanoateHCID 67075913—
Producttert-Butyl 3-(3-(1-ethyl-1H-pyrazol-4-yl)phenethoxy)propanoateHCID 59290442—

Reaction Steps

The subtitled compound (0.64 g) was prepared from tert-butyl 3-(3-bromophenethoxy)propanoate [Preparation 3, Step i)] and 1-ethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole using a similar method to that described in Example 18, Step i). MS[M+H-C4H8]+=289 (MultiMode+) 1H NMR (300 MHz, CDCl3) δ 7.76 (s, 1H), 7.65 (s, 1H), 7.35-7.23 (m, 3H), 7.07 (d, J=7.5 Hz, 1H), 4.21 (q, J=7.2 Hz, 2H), 3.70 (t, J=6.4 Hz, 2H), 3.68 (t, J=7.3 Hz, 2H), 2.89 (t, J=7.1 Hz, 2H), 2.49 (t, J=6.5 Hz, 2H), 1.53 (t, J=7.3 Hz, 3H), 1.43 (s, 9H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017602B2
Source datasetuspto-grants-2011_09
ORD IDord-2e1c02c12580474ab2f29213b55de161
Source noteuspto-grants-2011_09