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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426303Generated: October 26, 2026

2-(3-Benzyloxy-5-bromophenyl)malonic acid tert-butyl ester ethyl ester → (3-Benzyloxy-5-bromophenyl)-acetic acid ethyl ester

https://huagongshe.com/reaction/426303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Benzyloxy-5-bromophenyl)malonic acid tert-butyl ester ethyl esterHCID 66702482—
SolventAcetic AcidHCID 176—
Product(3-Benzyloxy-5-bromophenyl)-acetic acid ethyl esterHCID 66702483194.7%

Reaction Steps

2-(3-Benzyloxy-5-bromophenyl)malonic acid tert-butyl ester ethyl ester (7.2 g, contains 1.4 equivalent malonic acid tert-butyl ester ethyl ester, 10 mmol) was dissolved in glacial AcOH (50 mL) and heated to reflux for 12 h. The AcOH was removed under reduced pressure. The residue was poured into Na2CO3 solution (sat aq) and the mixture was extracted with EtOAc (×3). The combined organic extracts were washed with water, brine, dried (MgSO4), filtered and concentrated under reduced pressure to give (3-benzyloxy-5-bromo-phenyl-)acetic acid ethyl ester as a yellow liquid yield 6.8 g (97%). 1H NMR (CDCl3) δ 7.44-7.30 (m, 5H), 7.07-7.03 (m, 2H), 6.87-6.84 (m, 1H), 5.03 (s, 2H), 4.15 (q, 2H), 3.54 (s, 2H), 1.26 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106236B2
Source datasetuspto-grants-2012_01
ORD IDord-bd1343454b7f46c4aee1c886812d074d
Source noteuspto-grants-2012_01