HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366239Generated: October 28, 2026
Ethyl diazoacetate → (2-Bocamino-2-methyl-propoxy)-acetic acid
https://huagongshe.com/reaction/366239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)carbamate | HCID 14578673 | — |
| Catalyst | Acetic acid, rhodium(2+) salt | HCID 21674 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (2-Bocamino-2-methyl-propoxy)-acetic acid | HCID 10776871 | 38.2% |
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. Ethyldiazoacetate (4.0 g, 34.78 mmol) was slowly added over a period of 1 hr., and the mixture was stirred at reflux for 3 hr. Another 90 mg of rhodium(II)acetate was added and the mixture was refluxed for another 5 hr. The mixture was cooled overnight and 500 ml of saturated sodium bicarbonate was added, the yellow organic layer was separated and washed twice with saturated sodium bicarbonate (2×200 ml). The organic layer was dried over magnesium sulfate and concentrated in vacuo. The yellow oil was taken up in 200 ml of 1 M Lithium hydroxide in methanol:water (3:1) and stirred overnight. The solvent was removed in vacuo to a minimum and water was added (pH>9) and the mixture was washed with ether. Then 1 M hydrogen chloride was added until pH<4 and the mixture was extracted with ethyl acetate, dried over magnesium sulfate and concentrated in vacuo to give 2.5 g (38%) of (2-t-butoxycarbonylamino-2-methylpropoxy) acetic acid as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127391 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-e8fe0a132f28479ea15141c476e02c93 |
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| Source note | uspto-grants-2000_10 |
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