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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921669Generated: October 30, 2026

Lithium iodide → Tert-butyl 4-(1-aminocyclopropyl)benzoate

https://huagongshe.com/reaction/1921669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
ReactantTert-butyl 4-cyanobenzoateHCID 271408—
ReactantLithium propan-2-olateHCID 23673350—
ReactantHCID 178418750HCID 178418750—
CatalystHCID 178459133HCID 178459133—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductTert-butyl 4-(1-aminocyclopropyl)benzoateHCID 59305811—

Reaction Steps

50 mL of a 2M lithium isopropoxide solution in THF was placed under an argon atmosphere and 13.4 g of anhydrous lithium iodide was added thereto. After 15 minutes, 45 mL of a 1M methyltitanium isopropoxide solution in THF was added. Then the mixture was combined with 8.1 g of tert-butyl 4-cyanobenzoate and stirred for 10 minutes. Then within 60 minutes, 47.3 mL of a 15% diethylzinc solution in hexane was added thereto and the mixture was stirred for 12 hours at RT. After hydrolysis with 20 mL of water, it was stirred for a further 30 minutes, filtered off, and washed 3× with 100 mL of ether. After extraction of the organic phase with water, the mixture was evaporated down with silica gel and the substance was chromatographed with dichloromethane/methanol (98:2) at 20 mL/min on silica gel 70. Residue: 3 g oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173699B2
Source datasetuspto-grants-2012_05
ORD IDord-a90a8568033f448e96b5a8f58a54447f
Source noteuspto-grants-2012_05