HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602002Generated: October 28, 2026
Ethyl diazoacetate → HCID 10707551, compound
https://huagongshe.com/reaction/1602002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | tert-Butyl (1-hydroxybutan-2-yl)carbamate | HCID 15339785 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 10707551 | HCID 10707551 | 40% |
Reaction Steps
To a solution of (1-(hydroxymethyl)propyl)carbamic acid tert-butylester (7.2 g, 39 mmol) in 1,2-dichloroethane (500 ml) rhodium(II)acetate (180 mg) was added and the mixture was heated to 80° C. Ethyldiazoacetate (6.0 ml, 57 mmol) in 1,2-dichloroethane (180 ml) was added over a period of 60 min and the mixture was heated at 80° C. for 6 hours. Then another portion of ethyldiazoacetate (2.0 ml, 19 mmol) in 1,2-dichloroethane (40 ml) was added and the mixture was refluxed for 7 hours. The mixture was cooled to room temperature and washed with sodium bicarbonate (2×100 ml) and brine (100 ml), dried over magnesium sulfate and concentrated in vacuo. The crude product was chromatographed on silica (300 g) with pentane/ethyl acetate 7:3 as eluent to give 4.3 g of (2-(tert-butoxycarbonylamino)butoxy)acetic acid ethylester. The product was dissolved in of 1 M lithium hydroxide in water/methanol 1:3 (40 ml) and stirred at room temperature for 4 hours. The mixture was concentrated in vacuo and water (100 mL) was added and the solution was washed with ether (20 mL). The aqueous phase was acidified to pH 4 with 1M aqueous hydrogen chloride and extracted with ethyl acetate (200 ml), dried over magnesium sulfate and concentrated in vacuo to give 2.46 g of (2-(tert butoxycarbonylamino)butoxy)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977178 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-d557bc4b968b4b2dab933e9e7e1cd403 |
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| Source note | uspto-grants-1999_11 |
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