HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565008Generated: October 28, 2026
Ethyl Acetate → tert-Butyl [4-(hydroxymethyl)benzyl]carbamate
https://huagongshe.com/reaction/565008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Tert-butoxycarbonylaminomethyl)benzoate | HCID 6950640 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl [4-(hydroxymethyl)benzyl]carbamate | HCID 2794813 | 75.7% |
Reaction Steps
A suspension of 1.40 g (36.8 mmol) of lithium aluminum hydride in 150 ml of tetrahydrofuran was stirred at 0° C. A solution of 13.0 g (49.0 imol) of 4-(tert-butoxycarbonylaminomethyl)benzoate in 50 ml of tetrahydrofuran was dropwise added slowly to the suspension. After completion of the dropwise addition, the solution was heated to reflux for 2 hours and then cooled to 0° C. After 20 ml of 50% tetrahydrofuran was dropwise added to the reaction mixture, 100 ml of ethyl acetate was added thereto. Insoluble matters were filtered off and the resulting filtrate was concentrated under reduced pressure. The concentrate was isolated and purified by silica gel column chromatography to obtain 8.80 g (75.7%) of 4-(tert-butoxycarbonylaminomethyl)benzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-7e1e0045802f40348088c1580019fd3c |
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| Source note | uspto-grants-2001_01 |
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