HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115958Generated: November 4, 2026
Benzyl chloroformate → HCID 86599137, compound
https://huagongshe.com/reaction/2115958
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11960767 | HCID 11960767 | — |
| Product | HCID 86599137 | HCID 86599137 | 87.2% |
Reaction Steps
Treatment of (±)-1-[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methanamine (0.947 g, 3.73 mmol) with diisopropylethylamine (0.725 g, 5.60 mmol) and benzyl chloroformate (0.7647 g, 4.48 mmol) generally according to the procedure described for Intermediate 12 gave 1.26 g (87%) of (±)-benzyl[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate as a colorless oil Rf=0.56 (silica, ethyl acetate:hexanes 1:4); Anal. calcd. for C25H25NO3: C, 77.49; H, 6.50; N, 3.61. Found: C, 77.42H, 6.57; N, 3.62. Chiral HPLC separation of (±)-benzyl[7-(2,6-dimethylphenyl)-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate (Chiralcel OJ, methanol:carbon dioxide 4:6) provided two fractions. Fraction 1 (Rt=2.89 min, Chiralcel OJ, methanol:carbon dioxide 4:6); Fraction 2 (Rt=3.84 min, Chiralcel OJ, methanol:carbon dioxide 4:6).
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-566e757354b54c10b296bef63f93dc44 |
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| Source note | uspto-grants-2008_10 |
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