HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390120Generated: October 30, 2026
Sulfuric Acid → (1-Hydroxymethyl-2-vinylcyclopropyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/390120
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Ethyl 1-((tert-butoxycarbonyl)amino)-2-vinylcyclopropanecarboxylate | HCID 22091725 | — |
| Catalyst | Ammoniummolybdate cerium sulfate | HCID 131730262 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Hydroxymethyl-2-vinylcyclopropyl)-carbamic acid tert-butyl ester | HCID 68591817 | 96% |
Reaction Steps
To a solution of 1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acid ethyl ester (0.51 g, 2.0 mmol) in THF (10 ml) at 0° C. was added a 2M solution of lithiumborohydride (4 ml, 8 mmol). The reaction mixture was monitored by TLC (7:3 hexane-ethyl acetate, stained using ammoniummolybdate-cerium sulfate in aq. 10% sulfuric acid) and after stirring overnight at rt, the reaction was carefully quenched using aq. 10% citric acid (25 ml, dropwise addition at 0° C.). The obtained mixture was washed with dichloromethane (3×10 ml), and the combined org. layers were dried (Na2SO4), filtered and concentrated. Flash chromatography of the residue using 1:1 hexane-ethyl acetate as eluent, followed by concentration of the appropriate fractions and drying the residue in vacuum overnight, gave the product as a colorless syrup (0.407 g, 1.91 mmol, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383584B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-3dd61f6ea43a4bbf890bb7937bcb926b |
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| Source note | uspto-grants-2013_02 |
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