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
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 | 1,2-Dichloroethane | HCID 11 | — |
| Product | (2-Bocamino-2-methyl-propoxy)-acetic acid | HCID 10776871 | 38.9% |
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
| 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-9bff5072876b4f9b945d39c570d8933c |
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| Source note | uspto-grants-2000_10 |
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