HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115991Generated: October 31, 2026
Benzyl chloroformate → HCID 86599220, compound
https://huagongshe.com/reaction/2115991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11960945 | HCID 11960945 | — |
| Product | HCID 86599220 | HCID 86599220 | 81% |
Reaction Steps
Treatment of (±)-(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylamine (2.45 g, 8.11 mmol) with benzyl chloroformate (2.07 g, 12.15 mmol) and diisopropylethylamine (3.43 g, 24.32 mmol) generally according to the procedure described for Intermediate 12 provided 2.6 g (81%) of (±)-benzyl(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylcarbamate as a white solid. mp 90-92° C.; Anal. calcd. for C21H18ClNO3S: C, 63.07; H, 4.54; N, 3.50. Found: C, 63.44; H, 4.51; N, 3.43. Chiral HPLC separation of (±)-benzyl(5-chloro-7-thien-3-yl-2,3-dihydro-1-benzofuran-2-yl)methylcarbamate (Chiralpak AD, hexane:ethanol 1:1) provided two fractions. Fraction 1 (Rt=11.538 min, (Chiralpak AD, hexane:ethanol 1:1); Fraction 2 (Rt=17.694 min, (Chiralpak AD, hexane:ethanol 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-37826cedbde94d1f82d28a64d503b7e9 |
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| Source note | uspto-grants-2008_10 |
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