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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209434Generated: November 1, 2026

Diisopropylamine → HCID 86749013, compound

https://huagongshe.com/reaction/2209434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl bromoacetateHCID 60984—
Reactanttert-Butyl(dimethyl)silyl 3-phenylpropanoateHCID 554838—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86749013HCID 86749013—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve diisopropylamine (0.88 mL, 6.28 mmol) in tetrahydrofuran (7.5 mL). Cool in an ice bath and add, by dropwise addition, n-butyllithium (3.6 mL of a 1.6M solution in hexanes, 5.75 mmol). Stir for 15 minutes, then cool to -78° C. Add a solution of 3 -phenylpropionic acid, t-butyldimethylsilyl ester (1.33 g, 5.04 mmol) in tetrahydrofuran (5 mL). Stir for 45 minutes then add methyl bromoacetate (949 mg, 6.2 mmol). Stir for 3 hours, add saturated ammonium chloride (6 mL) and warm to room temperature. Partition between ethyl ether (75 mL) and water (10 mL). Dry (Na2SO4), evaporate the solvent in vacuo and purify by silica gel chromatography to give 3-phenyl-2-methylcarboxymethylpropionic acid, t-butyldimethylsilyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455242
Source datasetuspto-grants-1995_10
ORD IDord-cb13b4d6ae1948b5a30ea8c04ab21708
Source noteuspto-grants-1995_10