HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019358Generated: November 1, 2026
Chloromethyl-dimethyl-silane → HCID 18401194, compound
https://huagongshe.com/reaction/1019358
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl-dimethyl-silane | HCID 76597 | — |
| Reactant | tert-butyl N-(prop-2-en-1-yl)carbamate | HCID 4067274 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18401194 | HCID 18401194 | — |
Reaction Steps
A 250 mL 3-necked round bottom flask equipped with reflux condenser nitrogen inlet, thermometer heating mantle, pressure equalizing addition funnel and magnetic stirrer was charged with 14.36 g (91.3 mmol) of t-butyl N-allylcarbamate and 150 mL of toluene. The olefin and solvent were stirred and heated to about 70° C., then 10 microliters of Karstedt's catalyst (5% Pt solution, about 30 ppm Pt based on olefin) was added. A solution containing 12 g (110.5 mmol) of chloromethyldimethylsilane in 20 mL toluene was added cautiously over about 30 minutes at a rate sufficient to maintain the reaction temperature between about 80 and about 100° C. After addition was completed, the temperature was stirred and heated at about 85° for about 1 hour. GC-MS indicated complete reaction of the olefin to form the silylated compound, N-Boc-3-aminopropylchloromethyldimethylsilane. The solution was transferred to a 500 ml single neck round bottom flask and the solvent and excess silane were stripped via rotary evaporation to yield 25 g of crude product (quantitative yield based on olefin).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486364B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-ec159a51058d49f7b4f5485d438588d7 |
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| Source note | uspto-grants-2002_11 |
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