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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190889Generated: October 25, 2026

Water → HCID 58349494, compound

https://huagongshe.com/reaction/2190889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(4-Chlorophenyl)acetic acid tert-butyl esterHCID 13380183—
ReactantHCID 22399772HCID 22399772—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 58349494HCID 58349494—

Reaction Steps

To a suspension of KOtBu (980 mg, 8.73 mmol) in anhydrous DMF (15 mL) at 0° C. was added tert-butyl 4-chlorophenylacetate (1.80 g, 7.94 mmol). After stirring for two minutes, a solution of methyl 4-(1-bromobutyl)benzoate in DMF (5 mL) was added dropwise. The mixture was allowed to warm to room temperature. After stirring for 20 minutes, water was added then the solution was extracted with CH2Cl2 (2×100 mL). The combined organic layers were washed with saturated NH4Cl (aq) (20 mL) then saturated NaCl (aq) (20 mL), dried over Na2SO4, filtered, then concentrated. The residue was purified by silica gel chromatography eluting with 2% EtOAc/petroleum ether to afford the title compound: 1H NMR (300 MHz, CD3OD) δ 7.98-8.02 (m, 2 H), 7.77-7.81 (m, 2 H), 7.38-7.44 (m, 2 H), 7.09-7.13 (m, 2 H), 3.91 (s, 3 H), 3.79-3.81 (m, 1 H), 3.34-3.40 (m, 1 H), 1.20-1.30 (m, 2 H), 1.03 (s, 9 H), 0.91-1.02 (m, 2 H), 0.68 (t, J=7.4 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324384B2
Source datasetuspto-grants-2012_12
ORD IDord-19c1705728d846b481cb5975f1b55607
Source noteuspto-grants-2012_12