HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116057Generated: November 2, 2026
Benzyl chloroformate → HCID 86599145, compound
https://huagongshe.com/reaction/2116057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11961033 | HCID 11961033 | — |
| Product | HCID 86599145 | HCID 86599145 | 81% |
Reaction Steps
Treatment of (±)-1-[7-(2,4-difluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methanamine (2.0 g, 6.72 mmol) with diisopropylethylamine (1.30 g, 10.07 mmol) followed by benzyl chloroformate (1.26 g, 7.37 mmol) generally according to the procedure described for Intermediate 12 gave 2.14 g (81%) of (±)-benzyl {[7-(2,4-difluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methyl}carbamate as a white solid. mp 78-80° C.; Anal. calcd. for C23H19F2NO3: C, 69.87; H, 4.84; N, 3.54. Found: C, 69.76; H, 4.8; N, 3.35. Chiral HPLC separation of (±)-benzyl {[7-(2,4-difluorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methyl}carbamate (Chiralpak AD, ethanol:hexane 1:1) provided two fractions. Fraction 1 (Rt=9.117 min, Chiralpak AD, ethanol:hexane 1:1); Fraction 2 (Rt=9.424 min, Chiralpak AD ethanol:hexane 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435837B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-4743027ee9c5497abbc7cbb7d0d8e40e |
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| Source note | uspto-grants-2008_10 |
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