HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690698Generated: November 1, 2026
Methyl chloroformate → HCID 57618505, compound
https://huagongshe.com/reaction/1690698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 5-amino-2,3-dihydro-1H-inden-1-one | HCID 312890 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Water ethylacetate | HCID 22728543 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57618505 | HCID 57618505 | 89% |
Reaction Steps
To a suspension of 5-Amino-indan-1-one (commercially available, 100 mg, 0.679 mmol, 1 eq.) in a 2:1 v/v mixture of EtOAc/H2O (6 mL) is added NaHCO3 (114 mg, 1.36 mmol, 2 eq.). The resulting mixture is cooled to 0° C. followed by the addition of methyl chloroformate (0.052 mL, 0.679 mmol, 1 eq.). After stirring at 0° C. for 15 min., the reaction is warmed to 25° C. and stirred for 12 h. The reaction is diluted with EtOAc and sequentially washed with 1 N HCl (aq) and saturated aqueous NaCl. The resulting organic solution is dried over Na2SO4 and concentrated to give (1-Oxo-indan-5-yl)-carbamic acid methyl ester as a tan solid (124 mg, 89% yield). [MS: (ES+) 206.1 (M+1)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153671B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-72df77091fe04ba086879b535f644a4d |
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| Source note | uspto-grants-2012_04 |
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