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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366166Generated: October 26, 2026

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

https://huagongshe.com/reaction/366166

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—
Solvent1,1-DichloroethaneHCID 6365—
Product(2-Bocamino-2-methyl-propoxy)-acetic acidHCID 1077687138.2%

Reaction Steps

A solution of 2-t-butoxycarbonylamino-2-methylpropanol (5.0 g, 26.46 mmol) and rhodium(II)acetate (90 mg) in dichloroethane (500 ml) was heated to 80° C. Then ethyl diazoacetate (4.0 g, 34.78 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 layers were separated and the organic layer was washed twice with saturated sodium bicarbonate (2×200 ml) and 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 to a minimum, water (50 ml) was added (pH>9) and the mixture was washed with ether (100 ml). Then 1 M hydrochloric acid was added until pH<4 and the mixture was extracted with ethyl acetate (100 ml) and the combined organic layers were dried (magnesium sulfate) and concentrated in vacuo to give 2.5 g of (2-t-butoxycarbonylamino-2-methylpropoxy)acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127354
Source datasetuspto-grants-2000_10
ORD IDord-740cae675f8d40efbb58e10fbe3d0876
Source noteuspto-grants-2000_10