HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664216Generated: October 31, 2026
Isopropyl chloroformate → HCID 67441573, compound
https://huagongshe.com/reaction/1664216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67440676 | HCID 67440676 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 67441573 | HCID 67441573 | — |
Reaction Steps
5-Benzyloxycarbonylamino-isophthalic acid monomethyl ester (10 g, 30.1 mmol, 1 eq) and Et3N (5 ml, 36.1 mmol, 1.2 eq) are suspended in a mixture of THF (200 ml) and N-methylpyrrolidone (200 ml). Isopropylchloroformate (42 ml, 1 N in toluene, 42 mmol, 1.4 eq) is added, and the reaction mixture is stirred for 30 min at 0° C. and then diluted with diethyl ether and water. The organic layer is washed with 0.1 N HCl and brine. NaBH4 (3.82 g, 101 mmol, 3.36 eq) is dissolved in H2O (100 ml), and the solution is added to the reaction mixture, which is then stirred for 1 h. Diethyl ether and H2O are added, and the organic layer is separated, washed with brine, dried over sodium sulfate, filtered and concentrated. The residue is purified by column chromatography using EtOAc/hexane in a ratio of 1 to 2 to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039455B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-eff0631a95594f8aa4816f5c2a162510 |
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| Source note | uspto-grants-2011_10 |
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