HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39260Generated: October 25, 2026
Ethanolamine → 4-Acetoxybenzyl 2-hydroxyethylcarbamate
https://huagongshe.com/reaction/39260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetoxybenzyl 2-hydroxyethylcarbamate | HCID 58352638 | — |
Reaction Steps
A solution of butyl chloroformate (250 μL, 2 mmol) in 7 mL of CH2Cl2 was added to a mixture of ethanolamine (140 μL, 2.3 mmol) and triethylamine (540 μL, 3.9 mmol) in 7 mL of CH2Cl2 cooled in an ice bath. The mixture was stirred in the same bath, which was left unmaintained. After 5 h, it was diluted with 100 mL of ethyl acetate and washed with 50 mL of each of 1% HCl in 2/3 saturated brine, 2/3 saturated brine and saturated aqueous NaHCO3 (twice). The organics were dried over Na2SO4 and concentrated in vacuo to furnish 62 (318 mg, 2 mmol, quant.) as an oil. 1H NMR (400 MHz, CDCl3) δ 0.93 (t, J=7.4 Hz, 3H), 1.37 (sextet, J=7.4 Hz, 2H), 1.59 (pentet, J=7.2 Hz, 2H), 2.25 (broad s, 1H), 3.34 (broad q, J=5.2 Hz, 2H), 3.72 (broad q, J=4.8 Hz, 2H), 4.06 (t, J=6.6 Hz, 2H), 5.05 (broad s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524691B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-2b65a88c386a42d08e9b1587e0658f0b |
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| Source note | uspto-grants-2013_09 |
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