HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115946Generated: October 31, 2026
Benzyl chloroformate → HCID 91432033, compound
https://huagongshe.com/reaction/2115946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69274359 | HCID 69274359 | — |
| Product | HCID 91432033 | HCID 91432033 | — |
Reaction Steps
Treatment of (±)-benzyl(7-phenyl-2,3-dihydro-1-benzofuran-2-yl)methanamine (1.5 g, 1.43 mmol) with diisopropylethylamine (0.277 g, 2.14 mmol) followed by benzyl chloroformate (0.268 g, 1.572 mmol) generally according to the procedure described for Intermediate 12 provided 1.64 (79%) of (±)-benzyl[7-phenyl-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate as a clear oil. Rf=0.68 (silica, ethyl acetate:hexanes 1:2); Anal. calcd. for C23H21NO3: C, 76.86; H, 5.89; N, 3.90. Found: C, 75.10H, 5.71; N, 3.90. Chiral HPLC separation of (±)-benzyl[7-phenyl-2,3-dihydro-1-benzofuran-2-yl]methylcarbamate (Chiralpak AD, ethanol:hexane 1:1) provided two fractions. Fraction 1 (Rt=10.746 min, Chiralpak AD, ethanol:hexane 1:1); Fraction 2 (Rt=13.433 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-de5ea3faf1dc4f329eedc7e98e9b8092 |
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| Source note | uspto-grants-2008_10 |
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