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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366263Generated: October 29, 2026

Ethyl diazoacetate → (2-Bocamino-2-methyl-propoxy)-acetic acid

https://huagongshe.com/reaction/366263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl diazoacetateHCID 12192—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-(1-hydroxy-2-methylpropan-2-yl)carbamateHCID 14578673—
CatalystAcetic acid, rhodium(2+) saltHCID 21674—
Solvent1,2-DichloroethaneHCID 11—
Product(2-Bocamino-2-methyl-propoxy)-acetic acidHCID 1077687138.9%

Reaction Steps

A solution of 2 -tert-butoxycarbonylamino-2-methylpropanol (5.0 g, 26 mmol) and rhodium(II)acetate (90 mg) in 1,2-dichloroethane (500 ml) was heated to 80° C. Then ethyl diazoacetate (4.0 g, 35 mmol) was added over a period of 1 h, and the mixture was stirred at reflux for 3 h. Another portion of rhodium(II)acetate (90 mg) was added and the mixture was refluxed for another 5 h. The mixture was cooled overnight and saturated sodium bicarbonate (500 ml) was added, the phases were separated and the organic layer was washed with saturated sodium bicarbonate (2×200 ml), dried (magnesium sulfate) and concentrated in vacuo. The obtained product was dissolved in 1 M lithium hydroxide in methanol/water 3:1 (200 ml) and stirred overnight. The solvent was removed in vacuo, water was added (pH>9) and the mixture was washed with ether (200 ml). Then 1 M hydrochloric acid was added until pH<4 and the mixture was extracted with ethyl acetate (200 ml), dried (magnesium sulfate) and concentrated in vacuo to give 2.5 g of (2-tert-butoxycarbonylamino-2-methylpropoxy)acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127391
Source datasetuspto-grants-2000_10
ORD IDord-9bff5072876b4f9b945d39c570d8933c
Source noteuspto-grants-2000_10